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

HEPATIC FUNCTION ABNORMAL ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
CRYPTOPHTHALMOS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PYURIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MASS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
TOLOSA-HUNT SYNDROME ( 1 FDA reports)
TREMOR ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)

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