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

DRUG INEFFECTIVE ( 6 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
HEPATITIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
URTICARIA ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RASH ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
ANTI-PLATELET ANTIBODY ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)

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