Please choose an event type to view the corresponding MedsFacts report:

HEADACHE ( 6 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
VOMITING ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)

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