Kanarb | Adverse Reactions

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Full Prescribing Info

Adverse Reactions

The safety of Kanarb Tablets was evaluated in 406 patients, who had received Kanarb Tablets at the dose range of 60 to 120 mg for 4 to 12 weeks, out of a total of 852 patients with essential hypertension, enrolled in clinical trials and eligible for safety analysis (i.e., the safety database). There were 85 patients that received Kanarb Tablets for 6 months or longer. Most adverse events were mild to moderate, transient, and the occurrence rate was not related to dosage. The most frequently reported adverse events were headache and dizziness. Adverse reactions are summarized below (i.e., adverse events considered to be definitely related, probably related, or possibly related to Kanarb Tablets), reported in the clinical trials of Kanarb Tablets. (See Table.)

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Kanarb Adverse Reactions

Manufacturer:

Boryung Pharm

Distributor:

Zuellig Pharma