Cernevit Adverse Reactions

Concise Prescribing Info Full Prescribing Info Contents Description Action Indications/Uses Dosage/Direction for Use Overdosage Contraindications Warnings Special Precautions Use In Pregnancy & Lactation Adverse Reactions Drug Interactions Caution For Usage Storage MIMS Class ATC Classification Regulatory Classification Presentation/Packing

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Full Prescribing Info

Adverse Reactions

Adverse drug reactions (ADRs) that occurred after administration of Cernevit are presented with their relative frequencies; these include ADRs documented in clinical trials and those from post-marketing reports. Cernevit was administered during 3 clinical trials to 267 adult patients requiring a parenteral vitamin supplement.
Frequencies of ARs are reported, using the following convention: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1000 to <1/100); rare (≥1/10000 to <1/1000); very rare (<1/10000); and unknown (cannot be estimated from the available data).
Clinical Trial and Post-Marketing Adverse Drug Reactions Reported for Cernevit: See table as follows.

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Cernevit Adverse Reactions

Manufacturer:

Baxter Healthcare

Distributor:

Baxter Healthcare