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

WEIGHT INCREASED ( 103 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 63 FDA reports)
PANCREATITIS ( 30 FDA reports)
DYSPNOEA ( 26 FDA reports)
PNEUMONIA ( 23 FDA reports)
BLOOD CREATININE INCREASED ( 22 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
COGNITIVE DISORDER ( 16 FDA reports)
HYPERTENSION ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
CORONARY ARTERY DISEASE ( 15 FDA reports)
DEATH ( 15 FDA reports)
HYPOTENSION ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
OFF LABEL USE ( 13 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 11 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
ALBUMIN URINE PRESENT ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
POISONING ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CREATININE URINE INCREASED ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
INJURY ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
PAIN ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 5 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 5 FDA reports)
FALL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
OBESITY ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RASH ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
CREATINE URINE INCREASED ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MANIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIAC VALVE RUPTURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TONGUE PIGMENTATION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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