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

ERYTHEMA ( 5 FDA reports)
SWELLING FACE ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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