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

SKIN EXFOLIATION ( 5 FDA reports)
PRURITUS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
PAIN ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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