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

NAUSEA ( 11 FDA reports)
PAIN ( 7 FDA reports)
RENAL FAILURE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
RASH ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEAR ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
STRESS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYST ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LACERATION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POISONING ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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