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ACTIFED Safety Reports
Total ACTIFED reports: 3.ACTIFED FDA safety alerts: No.
Reported hospitalizations: 1.
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Consumer or non-health professional from UNITED STATES reported ACTIFED problem on Aug 10, 2006. Female patient, 84 years of age, weighting 93.00 lb, was diagnosed with hypersensitivity and was treated with ACTIFED. After drug was administered, patient experienced the following problems/side effects: breast pain, dyspnoea, palpitations. ACTIFED dosage: unknown. During the same period patient was treated with VITAMINS, ESTRADIOL, PROPRANOLOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.
ACTIFED problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 08, 2006. Male patient was treated with ACTIFED. After drug was administered, patient experienced the following problems/side effects: laryngeal cancer. ACTIFED dosage: unknown. Patient recovered.
Health Professional from PORTUGAL reported ACTIFED problem on Aug 28, 2007. Male patient, weighting 28.66 lb, was diagnosed with nasopharyngitis and was treated with ACTIFED. After drug was administered, patient experienced the following problems/side effects: hallucination, muscle spasms. ACTIFED dosage: 1.25 ML ONCE, ORAL. During the same period patient was treated with GUAIFENESIN, DEXCHLORPHENIRAMINE MALEATE, BETAMETHASONE, DROPROPIZINE. Patient recovered.