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

RENAL FAILURE ACUTE ( 62 FDA reports)
HYPOGLYCAEMIA ( 49 FDA reports)
DIARRHOEA ( 42 FDA reports)
RENAL FAILURE ( 39 FDA reports)
VOMITING ( 31 FDA reports)
ANAEMIA ( 30 FDA reports)
CHOLESTASIS ( 25 FDA reports)
HYPERKALAEMIA ( 25 FDA reports)
OEDEMA PERIPHERAL ( 22 FDA reports)
CYTOLYTIC HEPATITIS ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
LACTIC ACIDOSIS ( 21 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 20 FDA reports)
DYSPNOEA ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
FALL ( 18 FDA reports)
MALAISE ( 18 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
HYPONATRAEMIA ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
NAUSEA ( 15 FDA reports)
SEPTIC SHOCK ( 15 FDA reports)
WEIGHT INCREASED ( 15 FDA reports)
JAUNDICE ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
SHOCK ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
PRURITUS ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
ANURIA ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
HYPOGLYCAEMIC COMA ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
RASH ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ASCITES ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
ACIDOSIS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
VAGINAL CANCER ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
COMA ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FISTULA ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
NEPHROANGIOSCLEROSIS ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CITROBACTER TEST POSITIVE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HETEROPHORIA ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHLEBOTOMY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VIRAL TRACHEITIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-2 MACROGLOBULIN INCREASED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOXOCARIASIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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