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

ERYTHEMA ( 7 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
RASH ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
SKIN INFLAMMATION ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
DERMATITIS INFECTED ( 5 FDA reports)
ECZEMA HERPETICUM ( 5 FDA reports)
RASH PRURITIC ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GAZE PALSY ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
CRYING ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
PYODERMA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)

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