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

HYPOAESTHESIA ( 3 FDA reports)
RASH ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)

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