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Ocuvite Safety Reports
Total Ocuvite reports: 2.Ocuvite FDA safety alerts: No.
Reported hospitalizations: 2.
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Reported Ocuvite Side Effects: unresponsive to stimuli, decreased appetite, coronary artery occlusion, cardiac stress test abnormal, asthenia, amnesia, aggression, injection site bruising, heart rate increased, fatigue, diarrhoea.
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Ocuvite Side Effects Report #5164645-6
Consumer or non-health professional from UNITED STATES reported OCUVITE problem on Feb 17, 2006. Female patient, 78 years of age, was diagnosed with osteoporosis, arthritis and was treated with OCUVITE. After drug was administered, patient experienced the following problems/side effects: accidental overdose, anxiety, atrial fibrillation, cardiac flutter, contusion, diarrhoea, fatigue, heart rate increased, injection site bruising. OCUVITE dosage: unknown. During the same period patient was treated with FORTEO, FEMARA, TYLENOL, CALCIUM. Patient was hospitalized. Patient recovered.
Ocuvite Side Effects Report #5194792-4
OCUVITE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 19, 2006. Male patient was treated with OCUVITE. After drug was administered, patient experienced the following problems/side effects: aggression, amnesia, asthenia, cardiac stress test abnormal, coronary artery occlusion, decreased appetite, unresponsive to stimuli. OCUVITE dosage: unknown. During the same period patient was treated with VITMAMIN B, CATAPRES, FOLIC ACID, LIPITOR, PROTONIX, DILTIAZEM, LEXAPRO, ASPIRIN. Patient was hospitalized. Patient recovered.