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

DYSPNOEA ( 111 FDA reports)
RENAL FAILURE ( 86 FDA reports)
BLOOD CREATININE INCREASED ( 69 FDA reports)
RENAL FAILURE ACUTE ( 61 FDA reports)
BLOOD PRESSURE INCREASED ( 55 FDA reports)
HYPERTENSION ( 55 FDA reports)
PYREXIA ( 53 FDA reports)
BLOOD GLUCOSE INCREASED ( 49 FDA reports)
PNEUMONIA ( 48 FDA reports)
PAIN ( 46 FDA reports)
ANAEMIA ( 44 FDA reports)
CARDIAC FAILURE ( 44 FDA reports)
ASTHENIA ( 41 FDA reports)
COUGH ( 40 FDA reports)
FATIGUE ( 40 FDA reports)
DEATH ( 39 FDA reports)
MYOCARDIAL INFARCTION ( 39 FDA reports)
NAUSEA ( 39 FDA reports)
WEIGHT DECREASED ( 38 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 37 FDA reports)
HYPOTENSION ( 37 FDA reports)
BLOOD UREA INCREASED ( 36 FDA reports)
SEPSIS ( 36 FDA reports)
DIARRHOEA ( 34 FDA reports)
HAEMOPTYSIS ( 33 FDA reports)
MYALGIA ( 33 FDA reports)
PANCREATITIS ( 32 FDA reports)
DRUG INEFFECTIVE ( 30 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
HAEMOGLOBIN DECREASED ( 30 FDA reports)
CEREBROVASCULAR ACCIDENT ( 29 FDA reports)
CHEST PAIN ( 29 FDA reports)
CORONARY ARTERY DISEASE ( 29 FDA reports)
ANXIETY ( 27 FDA reports)
ARTHRALGIA ( 27 FDA reports)
DEHYDRATION ( 27 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
ANGINA PECTORIS ( 25 FDA reports)
ATRIAL FIBRILLATION ( 25 FDA reports)
MALAISE ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
VOMITING ( 25 FDA reports)
RENAL IMPAIRMENT ( 24 FDA reports)
INJURY ( 23 FDA reports)
ACUTE RESPIRATORY FAILURE ( 22 FDA reports)
FALL ( 22 FDA reports)
OEDEMA ( 22 FDA reports)
DIZZINESS ( 21 FDA reports)
MELAENA ( 21 FDA reports)
BACK PAIN ( 20 FDA reports)
CARDIAC ARREST ( 20 FDA reports)
CONFUSIONAL STATE ( 19 FDA reports)
HYPERKALAEMIA ( 19 FDA reports)
PAIN IN EXTREMITY ( 19 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
LETHARGY ( 18 FDA reports)
RENAL FAILURE CHRONIC ( 18 FDA reports)
WEGENER'S GRANULOMATOSIS ( 18 FDA reports)
ABASIA ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
UNEVALUABLE EVENT ( 17 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
DEPRESSION ( 16 FDA reports)
EJECTION FRACTION DECREASED ( 16 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
FEAR ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
INSOMNIA ( 16 FDA reports)
SYNCOPE ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
ASTHMA ( 15 FDA reports)
BRADYCARDIA ( 15 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
MICROALBUMINURIA ( 15 FDA reports)
PRURITUS ( 15 FDA reports)
RHABDOMYOLYSIS ( 15 FDA reports)
STRESS ( 15 FDA reports)
CORONARY ARTERY STENOSIS ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
JAUNDICE ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
AGITATION ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 13 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
HYPOXIA ( 13 FDA reports)
RENAL INJURY ( 13 FDA reports)
THROMBOSIS ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PANCREATITIS ACUTE ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 11 FDA reports)
GOUT ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
MOBILITY DECREASED ( 11 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
OSTEOARTHRITIS ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
STENT PLACEMENT ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HYPERSOMNIA ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
MALNUTRITION ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SPINAL COLUMN STENOSIS ( 9 FDA reports)
ASCITES ( 8 FDA reports)
ATELECTASIS ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
EAR PAIN ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
SWELLING ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ANGIOPLASTY ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
CATARACT ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
COLITIS ULCERATIVE ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
KNEE ARTHROPLASTY ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
RASH ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ANHEDONIA ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
COMA ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DIABETIC NEPHROPATHY ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GLOSSODYNIA ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAIR GROWTH ABNORMAL ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATOMEGALY ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
KNEE DEFORMITY ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NODAL OSTEOARTHRITIS ( 6 FDA reports)
NODULE ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
URINE ODOUR ABNORMAL ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANAL STENOSIS ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BONE DISORDER ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
CYST ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DENTAL OPERATION ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 5 FDA reports)
JOINT LOCK ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MESENTERIC OCCLUSION ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
NONINFECTIOUS PERITONITIS ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
OTITIS MEDIA ACUTE ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SENSORIMOTOR DISORDER ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SPONDYLOLISTHESIS ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
SYNOVIAL CYST ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BIOPSY SKIN ABNORMAL ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CORONARY ARTERY BYPASS ( 4 FDA reports)
CRYING ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
EHLERS-DANLOS SYNDROME ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEART VALVE INCOMPETENCE ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIMB DEFORMITY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
STEM CELL TRANSPLANT ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
APLASIA ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COAGULATION TIME ABNORMAL ( 3 FDA reports)
COELIAC ARTERY OCCLUSION ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POISONING ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY SEPSIS ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RICKETS ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SMALL INTESTINE GANGRENE ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BORRELIA BURGDORFERI SEROLOGY POSITIVE ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNOTACTOID GLOMERULONEPHRITIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLANTAR ERYTHEMA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL CANCER RECURRENT ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
WOUND ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER TUMOUR RESECTION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSECTING CORONARY ARTERY ANEURYSM ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATINURIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE URIC ACID ABNORMAL ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use