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

HYPOTENSION ( 16 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
DYSPNOEA ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
NAUSEA ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
CARDIOPULMONARY FAILURE ( 8 FDA reports)
CHILLS ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
DEATH ( 7 FDA reports)
FALL ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
WEGENER'S GRANULOMATOSIS ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMA ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KIDNEY MALROTATION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OBESITY ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPATORY FINDING ABNORMAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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