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

COMA ( 14 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
PYREXIA ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
BLISTER ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
SOMNOLENCE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
ANURIA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
APHONIA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)

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