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

DRUG INEFFECTIVE ( 41 FDA reports)
DYSPNOEA ( 37 FDA reports)
HEADACHE ( 20 FDA reports)
DRY MOUTH ( 19 FDA reports)
COUGH ( 15 FDA reports)
DIZZINESS ( 14 FDA reports)
HOARSENESS ( 14 FDA reports)
FATIGUE ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DYSPNOEA EXACERBATED ( 12 FDA reports)
NAUSEA ( 11 FDA reports)
RASH ( 11 FDA reports)
METRORRHAGIA ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
FALL ( 9 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
PAIN ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
BRONCHITIS ACUTE ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
VOMITING ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
AGEUSIA ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COMA ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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