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

MYOCARDIAL INFARCTION ( 33 FDA reports)
DEPRESSION ( 27 FDA reports)
ANXIETY ( 26 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
CEREBROVASCULAR ACCIDENT ( 18 FDA reports)
CORONARY ARTERY DISEASE ( 16 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
ERECTILE DYSFUNCTION ( 14 FDA reports)
ANGINA PECTORIS ( 13 FDA reports)
BACK PAIN ( 13 FDA reports)
INSOMNIA ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
DYSPEPSIA ( 11 FDA reports)
RHABDOMYOLYSIS ( 11 FDA reports)
DYSPNOEA ( 10 FDA reports)
GLOBAL AMNESIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
INFECTION ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
RASH ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEATH ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
FALL ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COMA ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIASTOLIC HYPERTENSION ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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