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LOSS OF CONSCIOUSNESS ( 6 FDA reports)
VOMITING ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
MALAISE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
COMA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RASH ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)

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