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

VOMITING ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
NAUSEA ( 7 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
DYSPHAGIA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
THIRST ( 5 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HERPES ZOSTER OTICUS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SPLENIC INJURY ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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