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

HYPERKALAEMIA ( 73 FDA reports)
RENAL FAILURE ACUTE ( 66 FDA reports)
HYPONATRAEMIA ( 37 FDA reports)
RENAL FAILURE ( 30 FDA reports)
DEHYDRATION ( 27 FDA reports)
FALL ( 24 FDA reports)
DIARRHOEA ( 23 FDA reports)
VOMITING ( 22 FDA reports)
ANAEMIA ( 21 FDA reports)
CONFUSIONAL STATE ( 21 FDA reports)
BRADYCARDIA ( 20 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
MALAISE ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
HYPOGLYCAEMIA ( 16 FDA reports)
METABOLIC ACIDOSIS ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
DYSPNOEA ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
ARRHYTHMIA ( 12 FDA reports)
LUNG DISORDER ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
COMA ( 10 FDA reports)
CYTOLYTIC HEPATITIS ( 10 FDA reports)
FACE OEDEMA ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
ANOREXIA ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
BRONCHITIS ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HYPOVOLAEMIA ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
COUGH ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ERYTHROSIS ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL ARTERY THROMBOSIS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPONTANEOUS HAEMATOMA ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WOUND ( 4 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PEDAL PULSE ABNORMAL ( 3 FDA reports)
PERIPHLEBITIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NECROSIS OF ARTERY ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE INFECTION TOXOPLASMAL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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