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

LOSS OF CONSCIOUSNESS ( 4 FDA reports)
RASH ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
CYTOMEGALOVIRUS TEST ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
PURPURA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
MELAENA ( 3 FDA reports)
PAIN ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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