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

RENAL FAILURE ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
URTICARIA ( 4 FDA reports)
TREMOR ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
TACHYCARDIA ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
CHILLS ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DEPRESSION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
DEATH ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
BED REST ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
FALL ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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