Yaz

Each hormone-containing, light pink, film-coated tablet contains 3.0 mg drospirenone and 0.020 mg ethinylestradiol stabilized by betadex as a clathrate (molecular inclusion complex).
YAZ (drospirenone and ethinylestradiol) tablets are available in a 28-day regimen.
Drospirenone: Proper Name: drospirenone.
Chemical Name: 6β, 7β; 15β, 16β-dimethylene-3-oxo-17α-pregn-4-ene-21,17-carbolactone (IUPAC) [6R-(6α, 7α, 8β, 9α, 10β, 13β, 14α, 15α, 16α, 17β]-1,3',4',6,7,8,9,10,11,12,13,14,15,16,20,21-hexadecahydro-10,13-dimethylspiro[17H-dicyclopropa[6,7:15,16] cyclopenta[α]phenanthrene-17,2'(5'H)-furan]-3,5'(2H)-dione (USAN).
Molecular Formula: C₂₄H₃₀O₃.
Molecular Weight: 366.50.
Description: White to off-white crystalline powder. Freely soluble in dichloromethane; soluble in acetone, methanol, ethyl acetate, dimethoxyethane and toluene; sparingly soluble in ethanol; and practically insoluble in water, n-hexane and diisopropyl ether. Melting range is 199°C to 201°C.
pKa: Neutral molecule without any acid-base properties in aqueous solutions (pH 1 to 12).
Partition coefficient: log P_OW = 3.08.
Ethinylestradiol: Proper Name: ethinylestradiol (as betadex clathrate).
Chemical Name: 19-nor-17α-pregna-1,3,5(10)-triene-20-yne-3,17-diol,Bis(β-cyclodextrin-clathrate) (IUPAC).
Molecular Formula: C₁₀₄H₁₆₄O₇₂.
Molecular Weight: 2566.4.
Description: White to off-white powder. The aqueous solubility of ethinyl estradiol (as betadex clathrate) is 3.7 g/L. Due to decomposition, no melting point or range can be determined.
pKa: 10.51 ± 0.03.
Partition Coefficient: log P_OW = 3.38 (pH=5); 3.53 (pH=7); 3.20 (pH=9).
Excipients/Inactive Ingredients: Nonmedicinal ingredients for hormone-containing tablets: lactose monohydrate, maize starch, magnesium stearate, lacquer pink (or alternatively hypromellose 5 cP, talc, titanium dioxide and ferric oxide red).
Nonmedicinal ingredients for hormone-free tablets: cellulose microcrystalline, lactose monohydrate, magnesium stearate, hypromellose 5 cP, talc, titanium dioxide.

Pharmacology: Mechanism of Action: YAZ is a monophasic, combination oral contraceptive that contains the progestin drospirenone (3.0 mg) and a low dose of the estrogen ethinyl estradiol (0.020 mg). Combination oral contraceptives act by suppression of gonadotropins. Although the primary mechanism of this action is inhibition of ovulation, other alterations include changes in the cervical mucus (which increases the difficulty of sperm entry into the uterus) and the endometrium (which reduces the likelihood of implantation).
Drospirenone is a spironolactone analogue with antimineralocorticoid activity. Preclinical studies in animals and in vitro have shown that drospirenone has no androgenic, estrogenic, glucocorticoid, and antiglucocorticoid activity. Preclinical studies in animals have also shown that drospirenone has antiandrogenic activity.
Estrogen-containing combinations such as YAZ increase the blood level of sex hormone binding globulin (SHBG), which is capable of binding and thus inactivating androgens such as testosterone. Moreover, the antiandrogenic activity of drospirenone partially counteracts the effects of endogenous androgens, blocking the binding of dihydrotestosterone (DHT) at the receptor level, which makes it a suitable option in the treatment of acne. Drospirenone may also help to reduce edema of the wall of the sebaceous follicle during the second half of the menstrual cycle, which is partly responsible for the flare-up of inflammatory lesions at this cycle phase.
Pharmacodynamics: Drospirenone inhibits ovulation and follicular development at an oral threshold dose of 2 mg. Drospirenone 3 mg in combination with ethinylestradiol was found to be optimal for inhibition of ovulation and cycle control. Administration of 3 extra days of hormone (YAZ 24-day active versus a 21-day active of the same combined oral contraceptive) results in additional suppression of the ovary and of follicular development. This was observed in a study where hormone-containing pills of each regimen were intentionally missed on the first 3 days of the cycle and subsequent follicular development was monitored.
Drospirenone exhibited aldosterone antagonist activity at doses as low as 2 mg/day in healthy volunteers. Plasma renin activity and plasma aldosterone concentrations were increased, as was the excretion of aldosterone metabolites. The excretion of Na⁺ was transiently increased by drospirenone (2 or 3 mg) alone or in combination with ethinylestradiol. Serum Na⁺ and K⁺ concentrations remained unchanged. The potency of drospirenone was 6.6 times higher on average than that of spironolactone, using the Na⁺/K⁺ urinary ratio as the primary indicator of potency of the aldosterone antagonistic effect.
Drospirenone (2, 3, or 4 mg) in combination with ethinylestradiol (0.020 mg) displayed a favourable effect on the lipid profile with an increase in HDL and a slight decrease in LDL. Total cholesterol remained unchanged. In addition, oral glucose tolerance was slightly increased, but remained within the reference range.
Drospirenone had no effect on the biosynthesis of SHBG, and when administered in conjunction with ethinylestradiol (0.020 mg), resulted in SHBG and corticosteroid binding globulin increases consistent with the dosage of ethinylestradiol.
In vitro, drospirenone bound with low affinity to SHBG and did not bind at all to corticosteroid binding globulin (CBG).
Clinical Trials: Contraception: General Information: The following table gives reported pregnancy rates for various forms of birth control, including no birth control. The reported rates represent the number of women out of 100 who would become pregnant in 1 year. (See Table 1.)

Click on icon to see table/diagram/image

Study Demographics and Trial Design: The contraceptive efficacy of YAZ (0.02 mg ethinylestradiol and 3 mg drospirenone/EE/DRSP) was evaluated in 2 pivotal phase III clinical trials. These studies (Studies 303740 and 308021) were large, open-label studies with the Pearl Index (PI) as primary criterion for the assessment of the contraceptive reliability.
Study 308020 was a comparison study with the following efficacy variables: cycle control, bleeding parameters, and the pregnancy rate expressed as PI.
An additional, single-center, controlled study (Study 301888) was conducted to investigate the impact of YAZ on plasma lipids, hemostatic variables and carbohydrate metabolism. Bleeding patterns were also assessed. (See Table 2.)

Click on icon to see table/diagram/image

Study Results: The total number of cycles under YAZ treatment in the two 13-cycle pivotal oral contraception studies was 24,818 (11,421 in Study 303740 and 13,397 in Study 308021). For Pearl Index (PI) calculations, 13/28-day cycles constitute 1 woman-year (wy). The pooled PI was calculated to be 0.85 with an upper one-sided 97.5% confidence limit of 1.39, and this is equal to the upper limit of the corresponding two-sided 95% confidence interval (CI). The PI was calculated based on the 16 pregnancies observed during YAZ treatment (Study 303740 with 11 pregnancies, PI=1.29 and Study 308021 with 5 pregnancies, PI=0.49) and a treatment exposure of 682,892 days (corresponding to 1,876.1 wy).
The adjusted Pearl Index (PI_c) in the YAZ studies was calculated on the basis of 7 pregnancies rated as method failure (5 in Study 303740 and 2 in Study 308021) and a treatment exposure of 581,408 days (corresponding to 1,597.2 wy). The PI was calculated to be 0.44 with an upper 2-sided 95% confidence limit of 0.90 (see Table 3). The individual study PI_c and upper 2-sided 95% confidence limit values were 0.72 and 1.69 for Study 303740, and 0.22 and 0.80 for Study 308021, respectively. (See Table 3.)

Click on icon to see table/diagram/image

In addition to the calculation of the PI, a life table analysis was performed for the time to the occurrence of a pregnancy in the two 13-cycle pivotal studies. The cumulative failure rate, ie, the probability of getting pregnant, was calculated using the Kaplan Meier estimator on the basis of unintended pregnancies considered to have occurred "during treatment."
The pooled Kaplan-Meier estimation after the last conception date after up to 1 year of treatment was 0.0085 with a 95% CI of 0.0052 to 0.0138, ie, the probability of contraceptive protection was estimated to be 0.9915 (99.15%). The estimation of the 1-year pregnancy rate for Study 303740 was 1.26% with a 95% CI of 0.0052 to 0.0201, and for Study 308021 this was 0.5% with a 95% CI of 0.0021 to 0.0119.
Bleeding Pattern: A multicenter, randomized, open, parallel-group study (Study 308020) was conducted to evaluate the bleeding pattern, cycle control, and contraceptive reliability of 0.02 mg EE/3 mg DRSP (EE/DRSP) versus 0.02 mg EE/150 mg DSG (EE/DSG). Female subjects were randomized to EE/DRSP (n=230) or EE/DSG (n=223) for 7 cycles.
The bleeding pattern was also evaluated in a multicenter, uncontrolled study (Study 303740) in which women were treated with EE/DRSP (n=890) for 13 cycles.
The bleeding episodes were described using the Reference Period method recommended by the World Health Organization (WHO). The length of the Reference Period is 90 days.
A bleeding/spotting episode was defined as a number of days with bleeding/spotting preceded and followed by at least 2 bleeding-free days; correspondingly, a spotting-only episode was defined as a number of days with spotting preceded and followed by at least 2 bleeding-free days. A bleeding-free interval consisted of at least 2 days without bleeding/spotting preceded and followed by at least 1 day of bleeding/spotting. Bleeding pattern evaluations are presented for the FAS using means and standard deviations (SD).
An overview of the bleeding pattern parameters for both treatment groups in Study 308020 is presented in Table 4 for Reference Period 1 and Reference Period 2. The mean values for all the parameters studied were very similar in both treatment groups.
The results were similar for the per protocol set (PPS). (See Table 4.)

Click on icon to see table/diagram/image

Bleeding pattern parameters for Study 303740 for Reference Periods 1 to 4 are presented in Table 5. (See Table 5.)

Click on icon to see table/diagram/image

The bleeding parameters (number of bleeding/spotting days, length of bleeding/spotting episodes and maximum length of bleeding/spotting episodes) decreased from Reference Period 1 to 2. After further treatment with YAZ, in Reference Periods 3 and 4, these bleeding parameters remained relatively stable at around the level of Reference Period 2. A similar pattern was observed in the analysis of spotting-only days and episodes.
The results were similar for the PPS.
Cycle Control: A summary of withdrawal and intracyclic bleeding data is presented in Table 6 for the 3 pivotal studies, based on the FAS population. (See Table 6.)

Click on icon to see table/diagram/image

Withdrawal Bleeding: Across all 3 studies, the majority of women had withdrawal bleeding. The percentage of volunteers with withdrawal bleeding was somewhat lower in cycle 1 (YAZ: 86.0% to 93.1% vs comparator: 75.9% to 87.1%) than in subsequent cycles, when at least 91.7% of subjects treated with YAZ and 92.3% of women in the comparator group experienced withdrawal bleeding.
The mean length of withdrawal bleeding decreased for both treatment groups from cycle 1 (YAZ: 5.2 to 7.3 days; comparator: 5.4 to 6.7 days) to cycle 6 (YAZ: 4.7 to 4.8 days; comparator: 5.2 to 5.3 days) with a slightly more pronounced decrease in the YAZ group. In the YAZ group, the mean length of withdrawal bleeding remained similar in cycle 9 (4.8 days), but further decreased to 2.6 days in cycle 13.
Intracyclic Bleeding: About one-quarter of the women in both the YAZ and comparator treatment groups of Studies 303740 and 301888 experienced intracyclic bleeding during cycle 1. In Study 308020, the withdrawal bleeding at study entry, on the first day of which the subjects had to take the first dose of study medication, was counted as intracyclic bleeding. Therefore, in this study the majority of women in both treatment groups had intermenstrual bleeding reported for cycle 1 (YAZ: 96.6%; comparator: 97.1%). However, across all studies and in both treatment groups the proportion of volunteers with intracyclic bleeding decreased to below one-fifth by cycle 6 (YAZ: 8.8% to 19.2%; comparator: 11.1% to 12.0%). With continued treatment, in the YAZ group the number of subjects who had intracyclic bleeding remained in the same range (cycle 9: 10.0%; cycle 13: 15.5%).
The mean length of intracyclic bleeding was similar between treatment groups and in general decreased from cycle 1 (YAZ: 4.7 to 8.4 days; comparator: 8.1 to 10.6 days) to cycle 6 (YAZ: 0.3 to 4.5 days; comparator: 0.5 to 5 days). In 1 study with longer YAZ treatment, the mean duration of intracyclic bleeding remained stable up to cycle 13 (4.5 to 4.8 days).
The mean number of intracyclic bleeding episodes per cycle was very low and varied between 0.1 and 1.4 for the YAZ-treated subjects and between 0.1 and 1.3 for the women in the comparator treatment group throughout the treatment period.
While more than one-half of women in both treatment groups experienced intracyclic bleeding of normal intensity in cycle 1, the predominant mean maximum intensity of intracyclic bleeding from cycle 2 onwards was spotting in both treatment groups. Intracyclic bleeding of normal and light intensity was equally distributed in most treatment cycles for both groups. Intracyclic bleeding of heavy intensity was only recorded for a few women.
From cycle 1 onwards, a decrease in the mean maximum length of intracyclic bleeding episodes was noted for YAZ and comparator-treated women. The mean maximum length of intracyclic bleeding episodes ranged from approximately 5 to 6 days from cycles 2 to 12 in the YAZ group and from 5 to 7 days in the comparator group from cycles 2 to 6.
The results were similar for the PPS.
Detailed Pharmacology: Animal Pharmacology: Drospirenone: Drospirenone exhibits potent progestational activity in a variety of animal models. In ovariectomized pregnant rats treated with drospirenone 3 mg/day sc in combination with ethinylestradiol 0.1 μg/day sc, maintenance of pregnancy was comparable to intact control animals. Drospirenone effectively inhibited ovulation in mice and rats with half-maximal effects observed at subcutaneous doses of approximately 0.1 and 1 mg/day, respectively, and an oral dose of 1 mg/day (rats). Following subcutaneous administration of drospirenone, a marked transformation of the endometrium was detected in castrated, infantile female rabbits, with a threshold dose of 100 to 300 μg/day. In vitro, drospirenone bound with high affinity to the progesterone receptor, and the binding affinity was not affected by the presence of ethinylestradiol.
In addition to its progestational activity, drospirenone also has antiandrogenic activity. Oral or subcutaneous administration of drospirenone (0.3 to 10 mg/day for 7 days) dose-dependently inhibited testosterone-induced growth of the seminal vesicle and prostate in castrated, testosterone-substituted rats. This activity does not appear to be centrally mediated in rats because decreases in the relative weights of male accessory sex organs occur in the absence of significant changes in testes weights or serum luteinizing hormone levels. Oral or subcutaneous administration of drospirenone (10 mg/day) to pregnant rats during the final trimester of pregnancy resulted in the feminization of male fetuses, characterized by a significant shortening of the anogenital distance and the length of the urethra.
Significant antimineralocorticoid activity, characterized by increased sodium excretion and an increase of the urinary Na⁺/K⁺ ratio, was observed following single oral or subcutaneous administration of drospirenone to adrenalectomized, aldosterone-substituted rats. Drospirenone was 5 to 10 times more potent than spironolactone, and its aldosterone antagonist activity was not affected by concomitant administration of ethinylestradiol. When administered for 21 days to ovariectomized female rats, drospirenone (10 mg/day) stimulated the Na⁺/K⁺ excretion ratio over the entire treatment period, while spironolactone (10 mg/day) became ineffective after the initial treatment phase due to counter-regulation. Drospirenone also exhibited significant antimineralocorticoid activity in vitro, inhibiting aldosterone-stimulated electrogenic sodium transport 10 times more effectively than either spironolactone or progesterone. In vitro, drospirenone binds with high affinity to the mineralocorticoid receptor.
Drospirenone has no androgenic activity. This was demonstrated in vitro by the lack of stimulation of androgen receptor-driven gene transcription. In vivo in castrated male rats, drospirenone (10 mg/day) did not stimulate the growth of accessory sex organs above castration level. The same dose had no virilizing effect on the process of sexual differentiation of female rat fetuses.
Drospirenone is devoid of estrogenic, gluco- and antiglucocorticoid activity, as concluded from the absence of an influence on vaginal epithelial cornification in rats, adrenal weight changes in rats, and thymus regression in adrenalectomized, glucocorticoid-substituted rats, respectively.
Drospirenone did not affect smooth muscle organs (ileum, trachea, uterus) in vivo (rabbit) or in vitro (guinea pigs). In female mice, drospirenone did not affect central nervous system function at single oral doses up to 100 mg/kg.
Drospirenone in subcutaneous doses of 1 or 10 mg/animal/day did not prevent hormone deficiency-induced trabecular bone loss in ovariectomized rats after treatment for 24 weeks. In addition, drospirenone in both tested doses did neither impair nor enhance the bone protective effect of ethinylestradiol on trabecular bone after 24 weeks of treatment.
When drospirenone (30 mg/kg/day) was subcutaneously administered to ovariectomized telemetered normotensive rats, only a slight increase in heart rate was found. However, this finding was not accompanied by any changes in systolic or diastolic blood pressure. The effects produced by 0.01 mg/kg/day ethinylestradiol (increased systolic blood pressure and lowered heart rate) were reduced when ethinylestradiol was coadministered with drospirenone. Drospirenone in subcutaneous doses of 1 or 10 mg/animal/day had no effect on liver-derived parameters (serum angiotensinogen and IGF-I) in ovariectomized rats after 11 treatment days.
In safety pharmacology studies, oral administration of drospirenone or drospirenone in combination with ethinylestradiol had no effect on pentylenetetrazole- or maximal electroshock-induced seizure activity in mice. When drospirenone was administered to rats as a single oral dose in combination with ethinylestradiol (100:1), a dose-dependent increase in urine volume and Na⁺ excretion, coupled with a dose-dependent decrease in urinary creatinine clearance, K⁺ and Cl^- excretion and BUN was observed. These effects on renal function were attributed to the antimineralocorticoid activity of drospirenone.
Ethinylestradiol: Ethinylestradiol is a potent estrogen with qualities similar to estradiol. In contrast to estradiol, it is highly effective after oral administration. The relative oral potency of ethinylestradiol's antigonadotropic and antifertility effects (eg, inhibition of ovulation, inhibition of implantation) is 3-30 times higher than that of orally administered estradiol.
Ethinylestradiol also exhibits effects on carbohydrate, protein, and lipid metabolism similar to those of other estrogens: in rats, hepatic glycogen content and serum triglycerides are significantly increased, whereas serum cholesterol is decreased. In addition, a small but significant increase in the liver weight can be seen. Phospholipids were also raised after treatment for 1 month. The effects on lipid and carbohydrate metabolism may be attributed to an indirect glucocorticoid activity of estrogens. It is well established that estrogens in the rat cause a stimulation of the adrenals and a depletion of corticoids. The increased glucocorticoid level may be responsible for an induction of gluconeogenesis concomitant with high fasting blood glucose levels.
Following administration of ethinylestradiol alone in ovariectomized rats, observations included dose-dependently higher uterine weights. Partial reversal of the stimulatory effect of ethinylestradiol on uterine weight was observed following administration of drospirenone (10 mg/animal/day) in combination with ethinyl estradiol (0.0001, 0.001 mg/animal/day).
Pharmacokinetics: See Table 7.

Click on icon to see table/diagram/image

Absorption: The absolute bioavailability of DRSP from a single entity tablet is about 76%. The absolute bioavailability of EE is approximately 40% as a result of presystemic conjugation and first-pass metabolism. The absolute bioavailability of YAZ which is a combination tablet of drospirenone and ethinylestradiol stabilized by betadex as a clathrate (molecular inclusion complex) has not been evaluated. The bioavailability of EE is similar when dosed via a betadex clathrate formulation compared to when it is dosed as a free steroid. Serum concentrations of DRSP and EE reached peak levels within 1 to 2 hours after administration of YAZ. After single dose administration of YAZ, the relative bioavailability compared to a suspension was 107% and 97% for DRSP and EE, respectively.
The pharmacokinetics of DRSP are dose proportional following single doses ranging from 1-10 mg. Following daily dosing of YAZ, steady-state DRSP concentrations were observed after 8 days. There was about 2- to 3-fold accumulation in serum C_max and AUC_(0-24h) values of DRSP following multiple-dose administration of YAZ.
For EE, steady-state conditions are reported during the second half of a treatment cycle. Following daily administration of YAZ, serum C_max and AUC_(0-24h) values of EE accumulate by a factor of about 1.5 to 2.0 (see Table 7).
Effect of Food: The rate of absorption of DRSP and EE following single administration of 2 tablets, each containing 3 mg DRSP and 0.030 mg EE was slower under fed conditions, with the serum C_max being reduced about 40% for both components. The extent of absorption of DRSP, however, remained unchanged. In contrast the extent of absorption of EE was reduced by about 20% under fed conditions.
Distribution: DRSP and EE serum levels decline in 2 phases. The apparent volume of distribution of DRSP is approximately 4 L/kg, and that of EE is reported to be approximately 4 to 5 L/kg.
DRSP does not bind to SHBG or CBG, but binds about 97% to other serum proteins. Multiple dosing over 3 cycles resulted in no change in the free fraction (as measured at trough levels). EE is reported to be highly but nonspecifically bound to serum albumin (approximately 98.5%) and induces an increase in the serum concentrations of both SHBG and CBG. EE induced effects on SHBG and CBG were not affected by variation of the DRSP dosage in the range of 2 to 3 mg.
Metabolism: The 2 main metabolites of DRSP found in human plasma were identified to be the acid form of DRSP, generated by opening of the lactone ring, and the 4,5-dihydrodrospirenone-3-sulfate, formed by reduction and subsequent sulfation. These metabolites were shown not to be pharmacologically active. DRSP is also subject to oxidative metabolism catalyzed by CYP3A4.
EE is subject to significant gut and hepatic first-pass metabolism. EE and its oxidative metabolites are primarily conjugated with glucuronides or sulfate. CYP3A4 in the liver are responsible for the 2-hydroxylation which is the major oxidative reaction. The 2-hydroxy metabolite is further transformed by methylation and glucuronidation prior to urinary and fecal excretion.
Excretion: DRSP serum levels are characterized by a terminal disposition phase half-life of approximately 30 hours after both single- and multiple-dose regimens. Excretion of DRSP was nearly complete after 10 days and amounts excreted were slightly higher in feces compared to urine. DRSP was extensively metabolized and only trace amounts of unchanged DRSP were excreted in urine and feces. At least 20 different metabolites were observed in urine and feces. About 38% to 47% of the metabolites in urine were glucuronide and sulfate conjugates. In feces, about 17% to 20% of the metabolites were excreted as glucuronides and sulfates.
For EE, the terminal disposition phase half-life has been reported to be approximately 24 hours. EE is not excreted unchanged. EE is excreted in the urine and feces as glucuronide and sulfate conjugates and undergoes enterohepatic circulation.
Special Populations and Conditions: Pediatrics: The safety and efficacy of YAZ has not been established in women under the age of 14 years. Use of this product before menarche is not indicated.
Geriatrics: YAZ is not indicated for use in postmenopausal women.
Race: No clinically significant difference was observed between the pharmacokinetics of DRSP or EE in Japanese versus Caucasian women (aged 20-35 years) when YAZ was administered daily for 21 days. The effect of race on the disposition of YAZ has not been evaluated.
Hepatic Insufficiency: YAZ is contraindicated in patients with hepatic dysfunction (see also Contraindications and Precautions). The mean exposure to DRSP in women with moderate hepatic impairment is approximately 3 times higher than the exposure in women with normal hepatic function. The mean terminal half-life of DRSP for women with moderate hepatic impairment was 1.8 times greater than for women with normal hepatic function. YAZ has not been studied in women with severe hepatic impairment.
Renal Insufficiency: YAZ is contraindicated in patients with renal insufficiency (see also Contraindications and Precautions).
The effect of renal insufficiency on the pharmacokinetics of DRSP (3 mg daily for 14 days) and the effect of DRSP on serum potassium levels were investigated in female subjects (n=28, age 30-65) with normal renal function and mild and moderate renal impairment. All subjects were on a low potassium diet. During the study, 7 subjects continued the use of potassium-sparing drugs for the treatment of the underlying illness. On the 14th day (steady-state) of DRSP treatment, the serum DRSP levels in the group with mild renal impairment (creatinine clearance CLcr, 50-80 mL/min) were comparable to those in the group with normal renal function (CLcr, >80 mL/min). The serum DRSP levels were on average 37% higher in the group with moderate renal impairment (CLcr, 30-50 mL/min) compared to those in the group with normal renal function. DRSP treatment was well tolerated by all groups. DRSP treatment did not show any clinically significant effect on serum potassium concentration. Although hyperkalemia was not observed in the study, in 5 of the 7 subjects who continued use of potassium-sparing drugs during the study, mean serum potassium levels increased by up to 0.33 mEq/L. Therefore, potential exists for hyperkalemia to occur in subjects with renal impairment whose serum potassium is in the upper reference range and who are concomitantly using potassium sparing drugs.
Toxicology: Acute Toxicity: Drospirenone: Table 8 as follows summarizes the median lethal doses (LD₅₀) determined in acute toxicity studies with drospirenone. (See Table 8.)

Click on icon to see table/diagram/image

The principle clinical signs observed in mice and rats were similar in all studies, including apathy, gait, and posture disturbances and at higher doses, twitching, spasms, and/or unconsciousness. Deaths generally occurred within 3 to 4 days of dosing.
Single high doses of drospirenone to female Beagle dogs were generally well tolerated, with compound-related effects limited to vomiting, transient changes in food/water consumption, and slight changes in serum biochemistry and coagulation parameters. No deaths occurred.
Long-term Toxicity: The long-term toxicity of drospirenone, alone and in combination with ethinylestradiol, was investigated after daily intragastric administration of the following doses. (See Table 9.)

Click on icon to see table/diagram/image

Compound related findings were generally limited to pharmacologic and exaggerated pharmacologic effects expected following administration of an exogenous progestogen or estrogen/progestogen combination. No organ toxicity was observed.
Changes observed following administration of drospirenone alone included: alterations in lipid, carbohydrate and protein metabolism (rats: ≥1 mg/kg/day); increased body weight gain and food consumption (rats: ≥3 mg/kg/day); decreased liver weights accompanied by decreased hepatic glycogen content (monkeys: ≥2 mg/kg/day); increased liver weights accompanied by increased hepatic DNA and protein content (rats: ≥50 mg/kg/day); changes in electrolyte excretion (rats: ≥10 mg/kg/day; monkeys: 10 mg/kg/day); decreased ovarian weights (mice: 30 mg/kg/day); decreased (mice: 30 mg/kg/day) or slightly increased (monkeys: 10 mg/kg/day) adrenal gland weights; microscopic changes in endocrine target organs (mice: ≥3 mg/kg/day; rats: ≥3 mg/kg/day; monkeys: ≥0.2 mg/kg/day).
A spectrum of compound-related estrogenic, progestogenic, and antimineralocorticoid effects was observed following administration of the combination to female mice, rats, and monkeys. In addition, the antagonism of some estrogenic effects (decreased body weight and food consumption [rats]; hematologic changes [rats, monkeys], and increased uterine weights [mice]), and antagonism of some progestogenic effects (increased body weight and food consumption [rats]) were observed.
Synergism of other effects was observed in mice and rats and included atrophy of ovarian interstitial glands, decreased luteal mass and sexual cycles in mice, and decreased ovarian weights and increased hepatic N-demethylase activity in rats. In comparison with administration of either substance alone, administration of the combination to rats and cynomolgus monkeys eliminated some single substance effects (alterations in hepatic cytochrome P450 content). Overt toxicity was limited to 1 possible compound-related death in cynomolgus monkeys administered the combination at a dose of 3 mg/kg drospirenone + 0.03 mg/kg ethinylestradiol for 11 weeks.
Toxicokinetic monitoring showed that on the basis of AUC_0-24h values, the highest doses used in mice (30 mg/kg/day), rats (15 mg/kg/day), and monkeys (10 mg/kg/day) which did not produce overt signs of toxicity led to roughly 10.6 times (mice), >12 times (rats), and ca 22 times (monkeys) higher systemic exposure as compared to human exposure at the therapeutic dose.
Carcinogenicity: The carcinogenic potential of drospirenone, alone and in combination with ethinylestradiol, was investigated in female mice and rats after daily intragastric administration of the following doses. (See Table 10.)

Click on icon to see table/diagram/image

No carcinogenicity was observed after 2 years of treatment with drospirenone as a single compound in mice or rats. Mortality was increased in rats at the highest dose of drospirenone. The increased food intake of the rats with a resultant increase in body weight was considered as the reason for the reduction in their life span. In the mouse study, there were no effects on the survival of the animals observed after treatment with drospirenone.
Tumorigenic effects of the drug combination in mice were manifested by an increased incidence of pituitary adenomas at all doses, overall mammary tumors at the mid and low doses, and uterine adenocarcinomas at the mid and high doses in comparison with controls. The same qualitative tumor pattern (however, quantitatively more pronounced, especially in the pituitary) was seen in groups treated with ethinylestradiol alone. As drospirenone alone elicited no tumorigenic response, the tumorigenic potential of the combination was attributed to ethinylestradiol.
Treatment of rats with the drug combination resulted in an increased incidence of hepatic adenomas at the high dose and of total liver tumors from the mid dose onwards. A similar effect on liver tumor induction was seen in groups receiving ethinylestradiol alone. Therefore, this effect on the liver could be attributed to the activity of ethinylestradiol.
Compared to the control group, a tendency towards an increased rate of endometrial adenoma with a concomitant decrease in the rate of adenocarcinoma was seen in the uteri from the animals of the low-dose combination group. In the mid- and high-dose combination groups, no endometrial adenomas or adenocarcinomas were noted, ie, there was a reduction in the rate of uterine tumors below the control level. A clear-cut increase in these uterine tumor incidences was induced by ethinylestradiol when given alone from the mid dose onwards. Thus, the presence of drospirenone in the drug combination apparently led to a suppression of the deleterious estrogenic effect on the uterus. Treatment with ethinylestradiol at the high dose led to an increased incidence of adenocarcinoma in the mammary glands. This effect was also completely counteracted by drospirenone in the drug combination group.
Evaluation of concomitant drug plasma concentrations revealed that exposure to drospirenone on the basis of AUC_0-24h values amounted to roughly 0.1-, 0.5-, and 3-fold multiples of human exposure after the low, mid, and high doses, respectively. The corresponding exposure multiples for drospirenone in the rat were approximately 0.5, 3.5, and 10 to 12 times human steady-state exposure.
Mutagenicity: No mutagenic effect of drospirenone was demonstrated in vitro in bacterial (Salmonella typhimurium, Escherichia coli) or mammalian (human lymphocyte, Chinese hamster) cells in the presence or absence of extrinsic metabolic activation. Drospirenone did not increase the occurrence of micronucleated red blood cells in vivo following single intragastric administration of 1000 mg/kg to mice.
Drospirenone increased unscheduled DNA synthesis in primary hepatocytes of female rats in vitro in a dose-dependent manner at a concentration of 10 to 60 μg/mL. Intragastric administration of drospirenone 10 mg/kg/day to rats for 14 consecutive days generated 2 forms of DNA adducts in male and female rat livers. Low levels of 3 compound-related DNA adducts were also observed in the livers of female mice given drospirenone 10 mg/kg/day, alone or in combination with 0.1 mg/kg/day ethinyl estradiol, in the carcinogenicity study. In contrast to these findings observed in rodent livers, results from an in vitro study conducted with drospirenone 5 μg/mL in human liver slices did not indicate a DNA adduct-forming potential of drospirenone in human tissue. Given the lack of any drospirenone-related liver tumor formation in mice and rats, the biological relevance of this interaction with DNA in the rodent liver with regard to risk assessment in humans is questionable.
Drospirenone did not demonstrate clastogenic potential in human lymphocytes in vitro at concentrations that were cytotoxic or precipitating in the presence or absence of extrinsic metabolic activation. No DNA adducts were detected in primary hepatocytes isolated from female rats incubated with 3.62 μM tritiated-drospirenone in vitro.
Based on the highest dose given in the mouse micronucleus study, the specification level of 0.1% and the expected maximum human intake of the impurity contained in a daily (3 mg) dose of drospirenone, the results of the mouse micronucleus test support a safety margin of 5 x 10⁵.
Following oral administration of drospirenone to juvenile rats for 5 days in a dose range-finding study, serum liver enzymes (aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase) were not altered at doses up to 500 mg/kg/day. Therefore, the high dose of 500 mg/kg/day was considered an adequate, nonhepatotoxic dose for a rat liver foci bioassay (which was subsequently cancelled for drospirenone when long-term data became available for drospirenone).
Reproduction and Teratology: The reproductive toxicity of drospirenone, alone and in combination with ethinylestradiol, was investigated in rats, rabbits, and monkeys following intragastric administration at the following doses: See Table 11.

Click on icon to see table/diagram/image

As expected from the pharmacological activity of an estrogen/progestogen combination, estrous cycle disturbances and a transient impairment of fertility were observed in rats when treated for 6 weeks prior to mating with doses of 5 mg/kg/day drospirenone + 0.05 mg/kg/day ethinylestradiol and higher. Pre- and postimplantation losses were significantly increased when 10 mg/kg/day drospirenone + 0.1 mg/kg/day ethinylestradiol were administered during the preimplantation phase of gestation in rats.
No teratogenicity was observed following intragastric administration of drospirenone, alone or in combination with ethinylestradiol, to female rats, rabbits and/or monkeys prior to mating or during gestation. Compound-related maternal toxicity characterized by decreased body weight gain (rats) and occasional vomiting (monkeys) was observed. The incidence of abortions was increased following administration of high doses of drospirenone (100 mg/kg/day) to pregnant rabbits, and a dose-dependent increase in abortions occurred following the administration of all doses to monkeys. Embryotoxicity and slight retardations of fetal development (eg, delayed ossification of feet bones, sternebrae, vertebrae; incomplete ossification of skull; slight increase in visceral abnormalities) were observed in the rat and rabbit at drospirenone doses of 15 mg/kg/day and 100 mg/kg/day, respectively.
Virilization of female fetuses (attributed to ethinylestradiol) and feminization of male fetuses (attributed to drospirenone) were observed following administration of the drug combination to pregnant rats on days 14 through 21 of pregnancy, beginning at doses of 5 + 0.05 mg/kg and 15 + 0.15 mg/kg, respectively. If exposure estimates from nonpregnant rats are extrapolated to pregnant animals, the administration of 15 mg/kg/day drospirenone would result in plasma exposure levels which are at least 10 times higher than the steady-state human exposure after intake of the drug product.
Prolonged or incomplete parturition or inability to deliver was observed when the drug combination was administered to rats from day 15 of gestation through day 3 postpartum. In the rat peri-/postnatal study, treatment from days 15 to 18 of gestation and days 1 to 22 postpartum caused a dose-dependent delay in postnatal development (body weight, physical, and functional parameters) and a dose-dependent increased mortality of the F1 offspring. These observations were attributed to the negative effects of drospirenone and/or ethinylestradiol on lactogenesis and milk secretion.
A reduced reproductive performance of the F₁ animals was observed at the dose of 45 mg/kg/day drospirenone + 0.45 mg/kg/day ethinylestradiol. This was attributed to an impairment of sex organ development in the male offspring due to the antiandrogenic activity of drospirenone.

YAZ (drospirenone and ethinylestradiol) is indicated for: Conception control.

Tablets must be taken in the order directed on the package every day at about the same time. The patient may begin using YAZ (drospirenone and ethinylestradiol) on day 1 of her menstrual cycle (ie, the first day of menstrual flow) or on the first Sunday after her period begins. If the patient's period begins on Sunday, she should start that same day. If YAZ tablets are taken later than day 1 when first starting medication, an additional (barrier) method of birth control is recommended for the first 7 days of use.
One hormone-containing light pink tablet is to be taken daily for 24 consecutive days, followed by 1 hormone-free white tablet daily for 4 consecutive days. Withdrawal bleeding usually occurs within 2 to 3 days following administration of the last hormone-containing light pink tablet (ie, while the patient is taking the hormone-free white tablets).
The patient begins each subsequent course of YAZ tablets on the same day of the week that she began her first course. She begins taking her next course immediately after completion of the last course, regardless of whether or not withdrawal bleeding is still in progress.
Management of missed tablets: The patient should be instructed to use the following chart if she misses 1 or more of her birth control pills. She should be told to match the number of tablets missed with the appropriate starting time for her dosing regimen. The risk of pregnancy increases with each hormone-containing light pink tablet missed. (See Table 12.)

Click on icon to see table/diagram/image

If the patient forgets any of the 4 hormone-free white tablets in week 4, she should be advised to safely dispose of the tablets she missed, and then to keep taking 1 tablet each day until the pack is empty. A back-up method of birth control is not required.
Special Notes on Administration: Switching from another combined hormonal contraceptive (combined oral contraceptive (COC), vaginal ring, or transdermal patch): The patient should start YAZ on the day she would normally start her next pack of combined oral contraceptive. In case a vaginal ring or transdermal patch has been used, the woman should start using YAZ preferably on the day of removal, but at the latest when the next application would have been due.
Switching from a progestin-only method (mini-pill, injection) or from a Progestin-releasing Intrauterine System (IUS): The patient may switch from the mini-pill to YAZ on any day of her cycle. Patients using a progestin injection should start YAZ on the day the next injection is due. Patients using an IUS should start YAZ on the day the IUS is removed. In all cases, the patient should be advised to use an additional (barrier) method for the first 7 days of YAZ use.
Following first trimester abortion: The patient may start using YAZ immediately. When doing so, she need not take additional contraceptive measures.
Following delivery or second trimester abortion: Patients should be advised to start YAZ on day 21 to 28 after delivery or second trimester abortion, after consulting with their physician. When starting later, the patient should be advised to use an additional (barrier) method for the first 7 days of YAZ use. However, if intercourse has already occurred, pregnancy should be excluded before the actual start of use, or the woman should be advised to wait for her next menstrual period prior to starting YAZ. When the tablets are administered in the postpartum period, the increased risk of thromboembolic disease associated with the postpartum period must be considered.
Withdrawal/breakthrough bleeding: Withdrawal bleeding usually occurs within 3 days following the last hormone-containing light pink tablet. If spotting or breakthrough bleeding occurs while taking YAZ, the patient should be instructed to continue taking YAZ as prescribed and by the regimen described previously. She should be instructed that this type of bleeding is usually transient and without significance; however, if the bleeding is persistent or prolonged, the patient should be advised to consult her physician.
Although the occurrence of pregnancy is unlikely if YAZ is taken according to directions, if withdrawal bleeding does not occur, the possibility of pregnancy must be considered. If the patient has not adhered to the prescribed dosing schedule (missed 1 or more hormone-containing tablets or started taking them on a day later than she should have), the probability of pregnancy should be considered at the time of the first missed period and appropriate diagnostic measures taken before the medication is resumed. If the patient has adhered to the prescribed regimen and misses 2 consecutive periods, pregnancy should be ruled out before continuing the contraceptive regimen.
Advice in case of vomiting: If vomiting occurs within 3 to 4 hours after a tablet is taken, absorption may not be complete. In such an event, the advice concerning management of missed tablets is applicable.

There have been no reports of overdose with YAZ (drospirenone and ethinylestradiol). Overdosage may cause nausea and vomiting, and withdrawal bleeding may occur in females. Withdrawal bleeding may even occur in girls before their menarche if they have accidentally taken the medicinal product. There are no antidotes and further treatment should be symptomatic based on the knowledge of the pharmacological action of the constituents. Drospirenone is a spironolactone analogue which has antimineralocorticoid properties. Serum concentration of potassium and sodium and evidence of metabolic acidosis should be monitored in cases of overdose. Liver function tests should be conducted, particularly transaminase levels, 2 to 3 weeks after consumption.

YAZ should not be used in women with: A history of or actual thrombophlebitis or thromboembolic disorders.
A history of or actual cerebrovascular disorders.
A history of or actual myocardial infarction or coronary artery disease.
Valvular heart disease with complications.
A history of or actual prodromi of a thrombosis (eg, transient ischemic attack, angina pectoris).
Presence of severe or multiple risk factor(s) for arterial or venous thrombosis: severe hypertension (persistent values of ≥160/100 mmHg); hereditary or acquired predisposition for venous or arterial thrombosis, such as Factor V Leiden mutation and activated protein C (APC) resistance, antithrombin-III-deficiency, protein C deficiency, protein S deficiency, hyperhomocysteinemia and antiphospholipid antibodies (anticardiolipin antibodies, lupus anticoagulant); severe dyslipoproteinemia; smoking, if over age 35; diabetes mellitus with vascular involvement; major surgery associated with an increased risk of postoperative thromboembolism; prolonged immobilization.
Use with the Hepatitis C virus combination drug regimen ombitasvir, paritaprevir, ritonavir, with or without dasabuvir (see Precautions).
Active liver disease or history of, or actual benign or malignant liver tumors.
Known or suspected carcinoma of the breast.
Carcinoma of the endometrium or other known or suspected estrogen-dependent neoplasia.
Undiagnosed abnormal vaginal bleeding.
Steroid-dependent jaundice, cholestatic jaundice, history of jaundice in pregnancy.
Any ocular lesion arising from ophthalmic vascular disease, such as partial or complete loss of vision or defect in visual fields.
Known or suspected pregnancy.
Current or history of migraine with focal aura.
History of or actual pancreatitis if associated with severe hypertriglyceridemia.
Renal insufficiency.
Hepatic dysfunction.
Adrenal insufficiency.
Hypersensitivity to this drug or to any ingredient in the formulation or component of the container. For a complete listing, see Description.

Cigarette smoking increases the risk of serious adverse effects on the heart and blood vessels. This risk increases with age, particularly in women over 35 years of age, and with the number of cigarettes smoked. For this reason, combination oral contraceptives, including YAZ, should not be used by women who are over 35 years of age and smoke. Women should be counselled not to smoke (see Cardiovascular under Precautions).
Hormonal contraceptives DO NOT PROTECT against sexually transmitted infections (STIs) including HIV/AIDS. While using hormonal contraceptives, it is advisable to use latex or polyurethane condoms IN COMBINATION WITH hormonal contraceptives to protect against STIs.

General: Discontinue Medication at the Earliest Manifestation of: A. Thromboembolic and Cardiovascular Disorders such as thrombophlebitis, pulmonary embolism, cerebrovascular disorders, myocardial ischemia, mesenteric thrombosis, and retinal thrombosis.
B. Conditions that Predispose to Venous Stasis and to Vascular Thrombosis (eg, immobilization after accidents or confinement to bed during long-term illness). Other nonhormonal methods of contraception should be used until regular activities are resumed. For use of oral contraceptives when surgery is contemplated, see Peri-operative Considerations as follows.
C. Visual Defects: Partial or Complete.
D. Papilledema, or Ophthalmic Vascular Lesions.
E. Severe Headache of Unknown Etiology or Worsening of Pre-existing Migraine Headache.
F. Increase in Epileptic Seizures.
The following information is provided from studies of combination oral contraceptives (COCs).
The use of combination hormonal contraceptives is associated with increased risks of several serious conditions including myocardial infarction, thromboembolism, stroke, hepatic neoplasia, and gallbladder disease, although the risk of serious morbidity and mortality is small in healthy women without underlying risk factors. The risk of morbidity and mortality increases significantly if associated with the presence of other risk factors such as hypertension, hyperlipidemias, obesity, and diabetes. Other medical conditions which have been associated with adverse circulatory events include systemic lupus erythematosus, hemolytic uremic syndrome, chronic inflammatory bowel disease, (Crohn's disease or ulcerative colitis), sickle cell disease, valvular heart disease, and atrial fibrillation.
The following conditions have been reported to occur or deteriorate with both pregnancy and COC use, although a direct association with COCs has not been firmly established: porphyria, systemic lupus erythematosus, hemolytic uremic syndrome, Sydenham's chorea, herpes gestationis, and otosclerosis-related hearing loss.
The information contained in this section is principally from studies carried out in women who used combination oral contraceptives with higher formulations of estrogens and progestins than those in common use today. The effect of long-term use of combination hormonal contraceptives with lower doses of both estrogen and progestin administered orally remains to be determined.
YAZ contains 3 mg of the progestin drospirenone (DRSP) that has antimineralocorticoid activity, including the potential for hyperkalemia in high-risk patients, comparable to a 25 mg dose of spironolactone. YAZ should not be used in patients with conditions that predispose to hyperkalemia (eg, renal insufficiency, hepatic dysfunction, and adrenal insufficiency). Women receiving daily, long-term treatment for chronic conditions or diseases with medications that may increase serum potassium should have their serum potassium level checked during the first treatment cycle. Drugs that may increase serum potassium include ACE inhibitors, angiotensin-II receptor antagonists, potassium-sparing diuretics, heparin, aldosterone antagonists, and NSAIDs.
Carcinogenesis and Mutagenesis: Malignancies may be life-threatening or may have a fatal outcome.
Breast Cancer: The frequency of diagnosis of breast cancer is very slightly increased among COC users. As breast cancer is rare in women under 40 years of age, the excess number is small in relation to the overall risk of breast cancer. Causation with COC use is unknown.
Increasing age and a strong family history are the most significant risk factors for the development of breast cancer. Other established risk factors include obesity, nulliparity, and late age for first full-term pregnancy. The identified groups of women that may be at increased risk of developing breast cancer before menopause are long-term users of oral contraceptives (more than 8 years) and starters at early age. In a few women, the use of oral contraceptives may accelerate the growth of an existing but undiagnosed breast cancer. Since any potential increased risk related to oral contraceptive use is small, there is no reason to change prescribing habits at present.
Women receiving oral contraceptives should be instructed in self-examination of their breasts. Their physicians should be notified whenever any masses are detected. A yearly clinical breast examination is also recommended, because, if breast cancer should develop, drugs that contain estrogen may cause a rapid progression.
Cervical Cancer: The most important risk factor for cervical cancer is persistent human papillomavirus infection (HPV). Some epidemiological studies have indicated that long-term use of COCs may further contribute to this increased risk, but there continues to be controversy about the extent to which this finding is attributable to confounding effects, eg, cervical screening and sexual behaviour including use of barrier contraceptives.
Hepatocellular Carcinoma: Hepatocelluar carcinoma may be associated with oral contraceptives. The risk appears to increase with duration of hormonal contraceptive use. However, the attributable risk (the excess incidence) of liver cancers in oral contraceptive users is extremely small. A liver tumor should be considered in the differential diagnosis when severe upper abdominal pain, liver enlargement or signs of intra-abdominal hemorrhage occur in women taking COCs.
See Pharmacology: Toxicology under Actions for discussion of animal data.
Cardiovascular: Predisposing Factors for Coronary Artery Disease: Cigarette smoking increases the risk of serious cardiovascular side effects and mortality. Birth control pills increase this risk, particularly in women over 35 years of age, and with the number of cigarettes smoked. Convincing data are available to support an upper age limit of 35 years for oral contraceptive use by women who smoke. For this reason, combination oral contraceptives, including YAZ, should not be used by women who are over 35 years of age and smoke.
Other women who are independently at high risk for cardiovascular disease include those with diabetes, hypertension, abnormal lipid profile, or a family history of these. Whether oral contraceptives accentuate this risk is unclear.
In low-risk, nonsmoking women of any age, the benefits of oral contraceptive use outweigh the possible cardiovascular risks associated with low-dose formulations. Consequently, oral contraceptives may be prescribed for these women up to the age of menopause.
Hypertension: Patients with essential hypertension whose blood pressure is well-controlled may be given hormonal contraceptives, but only under close supervision. If a significant elevation of blood pressure in previously normotensive or hypertensive subjects occurs at any time during the administration of the drug, cessation of medication is necessary. An increase in blood pressure has been reported in women taking COCs, and this increase is more likely in older women and with extended duration of use.
Endocrine and Metabolism: Diabetes: Current low-dose oral contraceptives exert minimal impact on glucose metabolism. Diabetic patients, or those with a family history of diabetes, should be observed closely to detect any worsening of carbohydrate metabolism. Patients predisposed to diabetes who can be kept under close supervision may be given oral contraceptives. Young diabetic patients whose disease is of recent origin, well-controlled, and not associated with hypertension or other signs of vascular disease such as ocular fundal changes, should be monitored more frequently while using oral contraceptives.
Lipid and Other Metabolic Effects: A small proportion of women will have adverse lipid changes while on oral contraceptives. Alternative contraception should be used in women with uncontrolled dyslipidemia (see also Contraindications). Elevations of plasma triglycerides may lead to pancreatitis and other complications.
Gastrointestinal: Published epidemiological studies indicate a possible association of COC use and the development of Crohn's disease and ulcerative colitis, although this has not been firmly established.
Genitourinary: Vaginal Bleeding: Persistent irregular vaginal bleeding requires assessment to exclude underlying pathology.
Fibroids: Patients with fibroids (leiomyomata) should be carefully observed. Sudden enlargement, pain, or tenderness requires discontinuation of the use of oral contraceptives.
Hematologic: Epidemiological studies have suggested an association between the use of COCs and an increased risk of arterial and venous thrombotic and thromboembolic diseases such as myocardial infarction, deep venous thrombosis, pulmonary embolism, and of cerebrovascular accidents. These events occur rarely.
The use of any combined oral contraceptive carries an increased risk of venous thromboembolism (VTE) compared with no use. The excess risk of VTE is highest during the first year a woman ever uses a combined oral contraceptive or restarts (following a 4-week or greater pill-free interval) the same or a different COC. Data from a large, prospective 3-armed cohort study suggest that this increased risk is mainly present during the first 3 months. VTE is life-threatening and is fatal in 1% to 2% of cases.
A large, prospective 3-armed cohort study has shown that the frequency of VTE diagnosis ranges from about 8 to 10 per 10,000 woman-years in users of oral contraceptives with low estrogen content (<50 μg ethinyl estradiol). The most recent data suggest that the frequency of VTE diagnosis is approximately 4.4 per 10,000 woman-years in nonpregnant, non-COC users and ranges from 20 to 30 per 10,000 woman-years in pregnant women or postpartum.
Overall the risk for VTE in users of oral contraceptives with low estrogen content (<50 μg ethinyl estradiol) is 2- to 3-fold higher than for nonusers of COCs who are not pregnant and remains lower than the risk associated with pregnancy and delivery.
The risk of VTE for combined oral contraceptives that contain drospirenone is higher than the risk for levonorgestrel-containing second generation COCs, and may be similar to the risk for desogestrel-containing or gestoden-containing third generation COCs.
Several epidemiological studies have examined the risk of VTE with drospirenone-containing COCs versus other COCs. Two prospective cohort studies showed that the risk of VTE with drospirenone-containing COCs is comparable to that of other COCs, including levonorgestrel-containing COCs. One case-control and three retrospective cohort studies suggested that the risk of VTE with drospirenone-containing COCs is higher compared to users of levonorgestrel-containing COCs. Two additional nested case-control studies have reported a two-fold and three-fold increased risk of idiopathic VTE in users of drospirenone-containing COCs as compared with levonorgestrel-containing COCs. These retrospective studies suggest a potential 1.5-3 times risk of VTE in users of drospirenone-containing COCs. Epidemiological studies have inherent methodological issues making the interpretation of their results complex. However, prescribers should consider the benefits and risks for specific patients with respect to VTE risk given the current retrospective epidemiological studies suggesting a higher risk of VTE with drospirenone-containing COCs compared to levonorgestrel-containing COCs.
VTE, manifesting as deep venous thrombosis (DVT) and/or pulmonary embolism (PE), may occur during the use of all COCs.
Extremely rarely, thrombosis has been reported to occur in other blood vessels (eg, hepatic, mesenteric, renal, cerebral, or retinal veins and arteries) in COC users.
Symptoms of DVT can include: unilateral swelling of the leg or along a vein in the leg; pain or tenderness in the leg, which may be felt only when standing or walking; increased warmth in the affected leg; red or discolored skin on the leg.
Symptoms of PE can include: sudden onset of unexplained shortness of breath or rapid breathing; sudden coughing which may bring up blood; sharp chest pain which may increase with deep breathing; sense of anxiety; severe light headedness or dizziness; rapid or irregular heartbeat. Some of these symptoms (eg, "shortness of breath", "coughing") are nonspecific and might be misinterpreted as more common or less severe events (eg, respiratory tract infections).
The risk for arterial thromboembolism (ATE) in users of oral contraceptives with low estrogen content (<50 μg ethinylestradiol) ranges from about 1 to 3 cases per 10,000 woman-years. An arterial thromboembolic event can include cerebrovascular accident, vascular occlusion, or myocardial infarction (MI). Symptoms of a cerebrovascular accident can include: sudden numbness or weakness of the face, arm, or leg, especially on one side of the body; sudden confusion, trouble speaking or understanding; sudden trouble seeing in one or both eyes; sudden trouble walking, dizziness, loss of balance or coordination; sudden, severe or prolonged headache with no known cause; loss of consciousness or fainting with or without seizure. Other signs of vascular occlusion can include: sudden pain, swelling, and slight blue discoloration of an extremity; acute abdomen.
Symptoms of MI can include: pain, discomfort, pressure, heaviness, sensation of squeezing or fullness in the chest, arm, or below the breastbone; discomfort radiating to the back, jaw, throat, arm, stomach; fullness, indigestion or choking feeling; sweating, nausea, vomiting, or dizziness; extreme weakness, anxiety, or shortness of breath; rapid or irregular heartbeats.
Arterial thromboembolic events are life-threatening and may have a fatal outcome.
Other Risk Factors for Venous or Arterial Thromboembolism or of a Cerebrovascular Accident: Other generalized risk factors for venous or arterial thromboembolism include but are not limited to age, severe obesity (body mass index >30 kg/m²), a personal history, a positive family history (the occurrence of VTE/ATE in a direct relative at a relatively early age may indicate genetic predisposition) and systemic lupus erythematosus. If a hereditary or acquired predisposition for venous or arterial thromboembolism is suspected, the woman should be referred to a specialist for advice before deciding on any COC use. The risk of VTE/ATE may be temporarily increased with prolonged immobilization, major surgery, or trauma. In these situations, it is advisable to discontinue COC use (in the case of elective surgery at least four weeks in advance) and not to resume COC use until 2 weeks after complete remobilization. Also, patients with varicose veins and leg cast should be closely supervised. Other risk factors may include smoking (with heavier smoking and increasing age, the risk further increases, especially in women over 35 years of age), dyslipoproteinemia, hypertension, migraine, valvular heart disease, and atrial fibrillation.
Biochemical factors that may be indicative of hereditary or acquired predisposition for venous or arterial thrombosis include Activated Protein C (APC) resistance, hyperhomocysteinemia, antithrombin-III deficiency, protein C deficiency, protein S deficiency, antiphospholipid antibodies (anticardiolipin antibodies, lupus anticoagulant).
When considering risk/benefit, the physician should take into account that adequate treatment of a condition may reduce the associated risk of thrombosis and that the risk associated with pregnancy is higher than that associated with low-dose COCs (<0.05 mg ethinylestradiol).
Hepatic/Biliary/Pancreatic: In some cases of elevated liver enzymes reported during clinical trials with YAZ, a contributory role of YAZ could not be ruled out. YAZ is contraindicated in patients with active liver disease (see Contraindications; Drug-Laboratory Test Interactions under Interactions).
Acute or chronic disturbances of liver function may necessitate the discontinuation of COC use until markers of liver function return to normal.
Jaundice: Patients who have had jaundice should be given oral contraceptives with great care and under close observation. Oral contraceptive-related cholestasis has been described in women with a history of pregnancy-related cholestasis. Women with a history of cholestasis may have the condition recur with subsequent hormonal contraceptive use.
The development of severe generalized pruritus or icterus requires that the medication be withdrawn until the problem is resolved.
If a patient develops jaundice that proves to be cholestatic in type, the use of oral contraceptives should not be resumed. In patients taking hormonal contraceptives, changes in the composition of the bile may occur and an increased incidence of gallstones has been reported.
Gallbladder Disease: Patients taking oral contraceptives have a greater risk of developing gallbladder disease requiring surgery within the first year of use. The risk may double after 4 or 5 years.
Hepatic Nodules: Hepatic nodules (adenoma and focal nodular hyperplasia) have been reported, particularly in long-term users of oral contraceptives. Although these lesions are extremely rare, they have caused fatal intra-abdominal hemorrhage and should be considered in women presenting with an abdominal mass, acute abdominal pain, or evidence of intra-abdominal bleeding.
Hepatitis C: YAZ must be discontinued prior to starting therapy with the Hepatitis C virus (HCV) combination drug regimen ombitasvir, paritaprevir, ritonavir, with or without dasabuvir (see Contraindications and Interactions). During clinical trials with ombitasvir, paritaprevir, ritonavir, with and without dasabuvir, ALT elevations 5 to >20 times the upper limit of normal (ULN) were significantly more frequent in healthy female subjects and HCV infected women using ethinyl estradiol-containing medications such as COCs. YAZ can be restarted approximately 2 weeks following completion of treatment with the HCV combination drug regimen.
Immune: Angioedema: Exogenous estrogens may induce or exacerbate symptoms of angioedema, in particular, in women with hereditary angioedema.
Neurologic: Migraine and Headache: The onset or exacerbation of migraine or the development of headache of a new pattern that is recurrent, persistent or severe, requires discontinuation of hormonal contraceptives and evaluation of the cause. Women with migraine headaches who take oral contraceptives may be at increased risk of stroke (see Contraindications).
Ophthalmologic: Ocular Disease: Patients who are pregnant or are taking oral contraceptives may experience corneal edema that may cause visual disturbances and changes in tolerance to contact lenses, especially of the rigid type. Soft contact lenses usually do not cause disturbances. If visual changes or alterations in tolerance to contact lenses occur, temporary or permanent cessation of wear may be advised.
Ocular Lesions: There have been clinical case reports of retinal thrombosis associated with the use of oral contraceptives. Oral contraceptives should be discontinued if there is unexplained partial or complete loss of vision, onset of proptosis or diplopia, papilledema, or retinal vascular lesions. Appropriate diagnostic and therapeutic measures should be undertaken immediately.
Peri-operative Considerations: There is an increased risk of thromboembolic complications in oral contraceptive users after major surgery. If feasible, oral contraceptives should be discontinued and an alternative method substituted at least 1 month prior to MAJOR elective surgery. Oral contraceptive use should not be resumed until the first menstrual period after hospital discharge following surgery.
Psychiatric: Patients with a history of emotional disturbances, especially the depressive type, may be more prone to have a recurrence of depression while taking oral contraceptives. In cases of a serious recurrence, a trial of an alternate method of contraception should be made, which may help to clarify the possible relationship. Women with premenstrual syndrome (PMS) may have a varied response to oral contraceptives, ranging from symptomatic improvement to worsening of the condition.
Renal: Fluid Retention: Hormonal contraceptives may cause some degree of fluid retention. They should be prescribed with caution and only with careful monitoring in patients with conditions which might be aggravated by fluid retention.
Sexual Function/Reproduction: Return to Fertility: After discontinuing oral contraceptive therapy, the patient should delay pregnancy until at least 1 normal spontaneous menstrual cycle has occurred in order to date the pregnancy. An alternate contraceptive method should be used during this time.
Amenorrhea: In some women, withdrawal bleeding may not occur during the tablet-free interval. If the COC has been taken according to directions, it is unlikely that the woman is pregnant. However, if the COC has not been taken according to directions prior to the first missed withdrawal bleed, or if two withdrawal bleeds are missed, pregnancy must be ruled out before COC use is continued.
Women having a history of oligomenorrhea, secondary amenorrhea, or irregular cycles may remain anovulatory or become amenorrheic following discontinuation of estrogen-progestin combination therapy.
Amenorrhea, especially if associated with breast secretion, that continues for 6 months or more after withdrawal, warrants a careful assessment of hypothalamic-pituitary function.
Reduced Efficacy: The efficacy of COCs may be reduced in the event of missed tablets, gastrointestinal disturbances or concomitant medication (see Dosage & Administration and Interactions).
Skin: Chloasma may occasionally occur with use of COCs, especially in women with a history of chloasma gravidarum. Women with a tendency to chloasma should avoid exposure to the sun or ultraviolet radiation while taking COCs.
Monitoring and Laboratory Tests: Physical Examination and Follow-up: Before oral contraceptives are used, a thorough history and physical examination should be performed, including a blood pressure determination and the family case history carefully noted. In addition, disturbances of the clotting system must be ruled out if any members of the family have suffered from thromboembolic diseases (eg, deep vein thrombosis, stroke, myocardial infarction) at a young age. Breasts, liver, extremities, and pelvic organs should be examined and a Papanicolaou (PAP) smear should be taken if the patient has been sexually active.
The first follow-up visit should be done 3 months after oral contraceptives are prescribed. Thereafter, examinations should be performed at least once a year, or more frequently if indicated. At each annual visit, examination should include those procedures that were done at the initial visit as previously outlined.
Use in Pregnancy: Oral contraceptives should not be taken by pregnant women. If pregnancy occurs during treatment with YAZ, further intake must be stopped. However, if conception accidentally occurs while taking the pill, there is no conclusive evidence that the estrogen and progestin contained in the oral contraceptive will damage the developing child. One infant was born with esophageal atresia during treatment with YASMIN, an OC of similar composition but with different dose and regimen. The causal association is unknown.
Use in Lactation: In breast-feeding women, the use of oral contraceptives results in the hormonal components being excreted in breast milk and may reduce its quantity and quality. If the use of oral contraceptives is initiated after the establishment of lactation, there does not appear to be any effect on the quantity and quality of the milk. There is no evidence that low-dose oral contraceptives are harmful to the nursing infant.
If possible, the nursing mother should be advised not to use oral contraceptives but to use other forms of contraception until she has completely weaned her child.
After oral administration of YASMIN, an OC of similar composition but with different dose and regimen, about 0.02% of the drospirenone dose was excreted into the breast milk of postpartum women within 24 hours. This results in a maximal daily dose of about 3 μg drospirenone in an infant.
Use in Children: The safety and efficacy of YAZ has not been established in women under the age of 14 years. Use of this product before menarche is not indicated.
Use in the Elderly: YAZ is not indicated for use in postmenopausal women.

Pregnant Women: Oral contraceptives should not be taken by pregnant women. If pregnancy occurs during treatment with YAZ, further intake must be stopped. However, if conception accidentally occurs while taking the pill, there is no conclusive evidence that the estrogen and progestin contained in the oral contraceptive will damage the developing child. One infant was born with esophageal atresia during treatment with YASMIN, an OC of similar composition but with different dose and regimen. The causal association is unknown.
Nursing Women: In breast-feeding women, the use of oral contraceptives results in the hormonal components being excreted in breast milk and may reduce its quantity and quality. If the use of oral contraceptives is initiated after the establishment of lactation, there does not appear to be any effect on the quantity and quality of the milk. There is no evidence that low-dose oral contraceptives are harmful to the nursing infant.
If possible, the nursing mother should be advised not to use oral contraceptives but to use other forms of contraception until she has completely weaned her child.
After oral administration of YASMIN, an OC of similar composition but with different dose and regimen, about 0.02% of the drospirenone dose was excreted into the breast milk of postpartum women within 24 hours. This results in a maximal daily dose of about 3 μg drospirenone in an infant.

Adverse Drug Reaction Overview: An increased risk of the following serious adverse reactions has been associated with the use of oral contraceptives: arterial and venous thromboembolism; being diagnosed with breast cancer; benign and malignant hepatic tumors; cerebral hemorrhage; cerebral thrombosis; congenital anomalies; gallbladder disease; hypertension; mesenteric thrombosis; myocardial infarction; neuro-ocular lesions (eg, retinal thrombosis); pulmonary embolism; thrombophlebitis.
The following adverse reactions also have been reported in patients receiving oral contraceptives: nausea and vomiting, usually the most common adverse reaction, occurs in approximately 10% or fewer of patients during the first cycle. The following other reactions, as a general rule, are seen less frequently or only occasionally: abdominal pain; amenorrhea during and after treatment; angioedema (exogenous estrogens may induce or exacerbate symptoms of angioedema in women with hereditary angioedema); auditory disturbances; breakthrough bleeding; breast changes (tenderness, enlargement and secretion); cataracts; changes in appetite; change in corneal curvature (steepening); changes in libido; change in menstrual flow; change in weight (increase or decrease); changes in glucose tolerance or effect on peripheral insulin resistance; chloasma or melasma which may persist; cholestatic jaundice; chorea; Crohn's disease; cystitis-like syndrome; mental depression; diarrhea; dizziness; dysmenorrhea; edema; endocervical hyperplasia; erythema multiforme; erythema nodosum; gallstone formation^a; gastrointestinal symptoms (such as abdominal cramps and bloating); headache; hemolytic uremic syndrome^a; hemorrhagic eruption; herpes gestationis^a; hirsutism; hypersensitivity; hypertriglyceridemia (increased risk of pancreatitis when using COCs); hypertension; impaired renal function; increase in size of uterine leiomyomata; intolerance to contact lenses; jaundice related to cholestasis^a; liver function disturbances; loss of scalp hair; migraine; nervousness; optic neuritis; otosclerosis-related hearing loss^a; pancreatitis; porphyria^a; possible diminution in lactation when given immediately postpartum; premenstrual-like syndrome; pruritus related to cholestasis^a; rash (allergic); Raynaud's phenomenon; reduced tolerance to carbohydrates; retinal thrombosis; rhinitis; spotting; Sydenham's chorea^a; systemic lupus erythematosus^a; temporary infertility after discontinuation of treatment; urticaria; ulcerative colitis; vaginal candidiasis; vaginal discharge; vaginitis.
^a Occurrence or deterioration of conditions for which association with COC use is not conclusive.
Clinical Trial Adverse Drug Reactions: Because clinical trials are conducted under very specific conditions the adverse reaction rates observed in the clinical trials may not reflect the rates observed in practice and should not be compared to the rates in the clinical trials of another drug. Adverse drug reaction information from clinical trials is useful for identifying drug-related adverse events and for approximating rates.
The clinical development programs were conducted independently for each of the 2 indications and utilized indication-specific inclusion criteria, study designs, and settings. Thus, the safety results of the studies are presented separately and are not pooled.
The following adverse drug reactions were reported at a frequency ≥ 1% in pivotal clinical trials using YAZ as an oral contraceptive: See Table 13.

Click on icon to see table/diagram/image

The following adverse drug reactions were reported at a frequency ≥1% in pivotal clinical trials using YAZ in the treatment of moderate acne vulgaris: See Table 14.

Click on icon to see table/diagram/image

Less Common Clinical Trial Adverse Drug Reactions: The following adverse drug reactions were seen at a frequency of <1% and ≥0.1% in pivotal clinical trials using YAZ as an oral contraceptive: Body as a whole: abdominal pain, asthenia, back pain, pain in extremity, pelvic pain.
Cardiovascular system: hypertension, migraine, varicose vein.
Digestive system: diarrhea, dyspepsia, flatulence, gastritis, vomiting.
Metabolic and nutritional disorders: weight gain, edema, peripheral edema.
Musculoskeletal system: muscle cramps.
Nervous system: dizziness, paresthesia, sweating increased, depression, libido decreased, nervousness, somnolence.
Skin and appendages: breast enlargement, acne, pruritus, fibrocystic breast, rash.
Urogenital system: hypomenorrhea, leukorrhea, vaginal dryness, vaginal moniliasis, dysmenorrhea, metrorrhagia, vaginal hemorrhage, menstrual disorder, PAP smear suspicious, vaginitis, menorrhagia.
The following adverse drug reactions were seen at a frequency of <1% and ≥0.1% in pivotal clinical trials using YAZ in the treatment of moderate acne vulgaris: Body as a whole: abdominal pain, asthenia, malaise.
Cardiovascular system: hypertension, migraine.
Urogenital system: amenorrhea, leukorrhea, PAP smear suspicious, uterine enlargement, vaginal moniliasis.
The following adverse drug reactions were seen at a frequency of <0.1% and ≥0.01% in pivotal clinical trials using YAZ as an oral contraceptive: Body as a whole: abdomen enlarged, accidental injury, allergic reaction, cyst, face edema, hernia, infection, moniliasis.
Cardiovascular system: phlebitis, syncope, tachycardia, vascular disorder.
Digestive system: biliary pain, cholecystitis, constipation, gastrointestinal disorder, gastrointestinal fullness, increased appetite, liver function test abnormal, oral moniliasis.
Endocrine system: endocrine disorder.
Metabolic and nutritional disorders: generalized edema, SGPT increased, weight loss.
Nervous system: hot flashes, insomnia, vertigo.
Respiratory system: epistaxis.
Skin and appendages: alopecia, breast neoplasm, chloasma, dermatitis acneiform, dry skin, eczema, erythema nodosum, hypertrichosis, skin disorder, skin striae.
Special senses: conjunctivitis, dry eye, eye disorder.
Urogenital system: anorgasmia, cervix neoplasm, dyspareunia, endometrial disorder, ovarian cyst, vulvovaginitis, withdrawal bleeding.
Postmarket Adverse Drug Reactions: The following unexpected adverse events have also been reported very rarely in users of YAZ, but a causal relationship has not been established: hot/cold sensations, muscle spasms, muscle twitching, and erythema multiforme.
In addition, venous and arterial thromboembolic events (peripheral deep venous occlusion, thrombosis and embolism/pulmonary vascular occlusion, thrombosis, embolism and infarction/myocardial infarction/cerebral infarction and stroke not specified as hemorrhagic) have been identified as Adverse Drug Reactions (ADRs) from postmarketing experience reported in association with the use of YAZ (see Contraindications; Hematologic under Precautions). Because these reactions are reported voluntarily from a population of uncertain size it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Overview: The concurrent administration of oral contraceptives with other may lead to breakthrough bleeding and/or may result in an altered response to either agent (see Table 15 and Table 16). Reduced effectiveness of the oral contraceptive, should it occur, is more likely with the low-dose formulations. It is important to ascertain all drugs that a patient is taking, both prescription and nonprescription, before oral contraceptives are prescribed.
Drug-Drug Interactions: See Table 15.

Click on icon to see table/diagram/image

Enzyme induction can already be observed after a few days of treatment. Maximal enzyme induction is generally seen within a few weeks. After the cessation of drug therapy enzyme induction may be sustained for about 4 weeks.
Women on short-term treatment with any of these drugs should temporarily use a barrier method in addition to the COC or choose another method of contraception. The barrier method should be used during the time of concomitant drug administration and for 28 days after their discontinuation. If the period during which the barrier method is used runs beyond the end of the hormone-containing light pink film-coated tablets in the COC pack, the hormone-free white film-coated tablets should be omitted and the next COC pack be started.
For women on long-term treatment with hepatic enzyme-inducing active substances, another reliable, non-hormonal, method of contraceptive is recommended.
Several of the anti-HIV/HCV protease inhibitors (eg, ritonavir, telaprevir, boceprevir) and nonnucleoside reverse transcriptase inhibitors (eg, nevirapine) have been studied with co-administration of oral combination hormonal contraceptives; significant changes (increase or decrease) in the mean AUC of the estrogen or progestin have been noted in some cases. The efficacy and safety of oral contraceptive products may be affected. Healthcare providers should refer to the label of the individual anti-HIV/HCV protease inhibitor for further drug-drug interaction information.
Strong and moderate CYP3A4 inhibitors such as azole antifungals (eg, ketoconazole, itraconazole, voriconazole, fluconazole), verapamil, macrolides (eg, clarithromycin, erythromycin), diltiazem and grapefruit juice, can increase plasma concentrations of the estrogen or the progestin or both. Increase in DRSP may increase serum potassium levels, possibly increasing the risk of hyperkalemia in high-risk patients (see General under Precautions).
Oral contraceptives may also interfere with the metabolism of other drugs (see Table 16). Accordingly, plasma and tissue concentrations may either increase (eg, cyclosporine) or decrease (eg, lamotrigine). (See Table 16.)

Click on icon to see table/diagram/image

In clinical studies, administration of a hormonal contraceptive containing ethinyl estradiol did not lead to any increase or only to a weak increase in plasma concentrations of CYP3A4 substrates (eg, midazolam) while plasma concentrations of CYP1A2 substrates can increase weakly (eg, theophylline) or moderately (eg, melatonin and tizanidine).
No formal drug-drug interaction studies have been conducted with ethinyl estradiol/drospirenone.
Interactions With Drugs That Have the Potential to Increase Serum Potassium: There is a potential for an increase in serum potassium in women taking YAZ with other drugs (see Precautions). Of note, occasional or chronic use of NSAID medication was not restricted in any of the YAZ clinical trials.
A drug-drug interaction study of DRSP 3 mg/estradiol 1 mg versus placebo was performed in 24 mildly hypertensive postmenopausal women taking enalapril maleate 10 mg twice daily. Potassium levels were obtained every other day for a total of 2 weeks in all subjects. Mean serum potassium levels in the DRSP/estradiol treatment group relative to baseline were 0.22 mEq/L higher than those in the placebo group. Serum potassium concentrations also were measured at multiple timepoints over 24 hours at baseline and on day 14. On day 14, the ratios for serum potassium C_max and AUC in the DRSP/estradiol group to those in the placebo group were 0.955 (90% CI: 0.914, 0.999) and 1.010 (90% CI: 0.944, 1.080), respectively. No patient in either treatment group developed hyperkalemia (serum potassium concentrations >5.5 mEq/L).
Drug-Food Interactions: Interactions with food have not been established.
Drug-Herb Interactions: Herbal products containing St. John's wort (Hypericum perforatum) may induce hepatic enzymes (cytochrome P450) and p-glycoprotein transporter and may reduce the effectiveness of contraceptive steroids. This may also result in breakthrough bleeding.
Drug-Laboratory Test Interactions: Results of laboratory tests should be interpreted with the knowledge that the patient is taking an oral contraceptive. The following laboratory tests are modified: A. Liver Function Tests: Aspartate serum transaminase (AST): variously reported elevations.
Alkaline phosphatase and gamma glutamine transaminase (GGT): slightly elevated.
B. Coagulation Tests: Minimal elevation of test values reported for such parameters as prothrombin and factors VII, VIII, IX, and X.
C. Thyroid Function Tests: Protein binding of thyroxine is increased as indicated by increased total serum thyroxine concentrations and decreased T₃ resin uptake.
D. Lipoproteins: Small changes of unproven clinical significance may occur in lipoprotein cholesterol fractions.
E. Gonadotropins: LH and FSH levels are suppressed by the use of oral contraceptives. Wait 2 weeks after discontinuing the use of oral contraceptives before measurements are made.
F. Glucose Tolerance: Oral glucose tolerance remained unchanged or was slightly decreased.
Tissue Specimens: Pathologists should be advised of oral contraceptive therapy when specimens obtained from surgical procedures and PAP smears are submitted for examination.
Drug-Lifestyle Interactions: No studies on the effects of YAZ on the ability to drive or use machines have been performed.
Metabolic Interactions: Drospirenone: Metabolism of drospirenone (DRSP) and potential effects of DRSP on hepatic cytochrome P450 (CYP) enzymes have been investigated in in vitro and in vivo studies (see Pharmacology: Pharmacokinetics: Metabolism under Actions). In in vitro studies, DRSP did not affect turnover of model substrates of CYP1A2 and CYP2D6, but had an inhibitory influence on the turnover of model substrates of CYP1A1, CYP2C9, CYP2C19, and CYP3A4, with CYP2C19 being the most sensitive enzyme. The potential effect of DRSP on CYP2C19 and CYP3A4 activity was investigated in clinical pharmacokinetic studies using omeprazole, simvastatin and midazolam as marker substrates. In a study with 24 postmenopausal women (including 12 women with homozygous [wild type] CYP2C19 genotype and 12 women with heterozygous CYP2C19 genotype), the daily oral administration of 3 mg DRSP for 14 days did not affect the oral clearance of omeprazole (40 mg, single oral dose). Two additional clinical drug-drug interaction studies using simvastatin and midazolam as marker substrates for CYP3A4 were each performed in 24 healthy postmenopausal women. The results of these studies demonstrated that pharmacokinetics of the CYP3A4 substrates were not influenced by steady state DRSP concentrations achieved after administration of 3 mg DRSP/day. Based on the available results of in vivo and in vitro studies, it can be concluded that, at clinical dose levels, DRSP shows little propensity to interact to a significant extent with cytochrome P450 enzymes.
Ethinylestradiol: In vitro, ethinylestradiol is a reversible inhibitor of CYP2C19, CYP1A1 and CYP1A2 as well as a mechanism based inhibitor of CYP3A4/5, CYP2C8, and CYP2J2.

Special Handling Instructions: There are no special handling instructions.

Store below 25 °C. Store in the original package.
Medicines should not be disposed of via wastewater or household waste. Ask the pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

Oral Contraceptives

G03AA12 - drospirenone and ethinylestradiol ; Belongs to the class of progestogens and estrogens in fixed combinations. Used as systemic contraceptives.

NP