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

FLUSHING ( 21 FDA reports)
NAUSEA ( 19 FDA reports)
DIZZINESS ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
VOMITING ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
HYPOTENSION ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
HYPERCHOLESTEROLAEMIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
ANXIETY ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
ASTHMA ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
COUGH ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
NEPHROPATHY ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
ADNEXA UTERI CYST ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
PAIN ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
TREMOR ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OBESITY ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
INJURY ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CRYING ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
RASH ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ANHEDONIA ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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