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ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
T-CELL LYMPHOMA ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
INFECTION ( 4 FDA reports)
BREAST CANCER ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BUNION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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