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

HYPONATRAEMIA ( 55 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 47 FDA reports)
FALL ( 43 FDA reports)
ASTHENIA ( 41 FDA reports)
PYREXIA ( 41 FDA reports)
RENAL FAILURE ( 41 FDA reports)
VOMITING ( 37 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
NAUSEA ( 32 FDA reports)
CONFUSIONAL STATE ( 31 FDA reports)
DRUG INTERACTION ( 30 FDA reports)
MALAISE ( 30 FDA reports)
TREMOR ( 27 FDA reports)
ANAEMIA ( 25 FDA reports)
SOMNOLENCE ( 24 FDA reports)
DIARRHOEA ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
DEHYDRATION ( 22 FDA reports)
HYPOKALAEMIA ( 22 FDA reports)
HYPOPHAGIA ( 22 FDA reports)
ANOREXIA ( 21 FDA reports)
ARTHRALGIA ( 21 FDA reports)
HYPERKALAEMIA ( 21 FDA reports)
VERTIGO ( 21 FDA reports)
BACK PAIN ( 19 FDA reports)
BRONCHITIS ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
DISORIENTATION ( 18 FDA reports)
DYSPHAGIA ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
HYPOTENSION ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
POLYNEUROPATHY ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
DEPRESSION ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
INSOMNIA ( 15 FDA reports)
PAIN ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
OEDEMA ( 14 FDA reports)
ORAL PAIN ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
CHOLESTASIS ( 13 FDA reports)
DYSGEUSIA ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
RASH ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
OESOPHAGITIS ( 12 FDA reports)
ORTHOSTATIC HYPOTENSION ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
THROMBOCYTOSIS ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
ARTHRITIS ( 11 FDA reports)
ATAXIA ( 11 FDA reports)
ATELECTASIS ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
BONE DISORDER ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
CEREBRAL ATROPHY ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DEAFNESS ( 11 FDA reports)
DECREASED INTEREST ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
EMOTIONAL DISTRESS ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
EMPYEMA ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
HALLUCINATION ( 11 FDA reports)
HEPATIC CYST ( 11 FDA reports)
IMPAIRED HEALING ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
LIFE EXPECTANCY SHORTENED ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
MUSCULOSKELETAL PAIN ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
SINUS DISORDER ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
SWELLING FACE ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
EOSINOPHILIA ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
RENAL IMPAIRMENT ( 10 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CATARACT ( 8 FDA reports)
DUODENITIS ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
EYE PAIN ( 8 FDA reports)
EYELID PTOSIS ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HYPERMETROPIA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
APHASIA ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HYPOCHLORAEMIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
COR PULMONALE CHRONIC ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
AGGRESSION ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
COMA ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
RALES ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
SHOCK ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOCAPNIA ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
WEGENER'S GRANULOMATOSIS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTHRITIS SALMONELLA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CORTISOL INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COUGH ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH SCALY ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
DACRYOCYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
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HERPES DERMATITIS ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
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HYPOGLYCAEMIC COMA ( 1 FDA reports)
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HYPOREFLEXIA ( 1 FDA reports)
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IMPETIGO ( 1 FDA reports)
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INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
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KETONURIA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHLEBITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYP ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
RADIATION INTERACTION ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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