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

URTICARIA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
HYPOTENSION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYANOSIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FALL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
APNOEA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)

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