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

COUGH ( 33 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 31 FDA reports)
FIBROSIS ( 31 FDA reports)
HYPERTENSION ( 30 FDA reports)
DIARRHOEA ( 28 FDA reports)
PAIN ( 28 FDA reports)
ANXIETY ( 27 FDA reports)
DYSPNOEA ( 27 FDA reports)
EMOTIONAL DISTRESS ( 27 FDA reports)
PALPITATIONS ( 27 FDA reports)
INJURY ( 26 FDA reports)
MALAISE ( 26 FDA reports)
OSTEOARTHRITIS ( 26 FDA reports)
SPINAL OSTEOARTHRITIS ( 26 FDA reports)
CONSTIPATION ( 25 FDA reports)
MYALGIA ( 25 FDA reports)
DISCOMFORT ( 24 FDA reports)
HEART RATE INCREASED ( 24 FDA reports)
MUSCULOSKELETAL PAIN ( 24 FDA reports)
SCAR ( 24 FDA reports)
ANHEDONIA ( 23 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 23 FDA reports)
DECREASED APPETITE ( 23 FDA reports)
DRY MOUTH ( 23 FDA reports)
DYSPHONIA ( 23 FDA reports)
FALL ( 23 FDA reports)
FEELING JITTERY ( 23 FDA reports)
FRACTURED SACRUM ( 23 FDA reports)
GINGIVAL BLEEDING ( 23 FDA reports)
GOITRE ( 23 FDA reports)
HEART RATE IRREGULAR ( 23 FDA reports)
HYPOPHAGIA ( 23 FDA reports)
INFLUENZA ( 23 FDA reports)
NODULE ( 23 FDA reports)
OROPHARYNGEAL PAIN ( 23 FDA reports)
OSTEOLYSIS ( 23 FDA reports)
OSTEOMYELITIS ( 23 FDA reports)
OSTEOPENIA ( 23 FDA reports)
PAIN IN JAW ( 23 FDA reports)
SJOGREN'S SYNDROME ( 23 FDA reports)
SPEECH DISORDER ( 23 FDA reports)
TOOTH IMPACTED ( 23 FDA reports)
BONE DISORDER ( 22 FDA reports)
CHRONIC SINUSITIS ( 22 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 22 FDA reports)
GINGIVAL DISORDER ( 22 FDA reports)
GINGIVAL HYPERPLASIA ( 22 FDA reports)
GINGIVAL OEDEMA ( 22 FDA reports)
GINGIVITIS ( 22 FDA reports)
ISCHAEMIA ( 22 FDA reports)
LIFE EXPECTANCY SHORTENED ( 22 FDA reports)
LIPIDS INCREASED ( 22 FDA reports)
MITRAL VALVE INCOMPETENCE ( 22 FDA reports)
MUCOSAL DRYNESS ( 22 FDA reports)
RESPIRATORY DISORDER ( 22 FDA reports)
STOMATITIS ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
FISTULA ( 21 FDA reports)
GINGIVAL RECESSION ( 21 FDA reports)
JAW DISORDER ( 21 FDA reports)
OROPHARYNGEAL PLAQUE ( 21 FDA reports)
PHYSICAL DISABILITY ( 21 FDA reports)
BACK PAIN ( 20 FDA reports)
DIZZINESS ( 20 FDA reports)
CELLULITIS ( 19 FDA reports)
VITREOUS HAEMORRHAGE ( 18 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
TREMOR ( 17 FDA reports)
EAR HAEMORRHAGE ( 16 FDA reports)
FACIAL PAIN ( 16 FDA reports)
LARYNGEAL OEDEMA ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
REFLUX OESOPHAGITIS ( 16 FDA reports)
SICCA SYNDROME ( 16 FDA reports)
THYROID ADENOMA ( 15 FDA reports)
THYROID NEOPLASM ( 15 FDA reports)
INFLAMMATION ( 14 FDA reports)
NECK PAIN ( 14 FDA reports)
BONE DENSITY DECREASED ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
OSTEONECROSIS OF JAW ( 13 FDA reports)
ACUTE SINUSITIS ( 12 FDA reports)
CONTUSION ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
DENTAL IMPLANTATION ( 12 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
HIATUS HERNIA ( 12 FDA reports)
LACERATION ( 12 FDA reports)
ANGIOPATHY ( 11 FDA reports)
BONE DEBRIDEMENT ( 11 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 11 FDA reports)
IMPETIGO ( 11 FDA reports)
MEDICAL DEVICE REMOVAL ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
ORAL SURGERY ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
SPINAL CORD DISORDER ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
BONE LOSS ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
HYPERTONIC BLADDER ( 10 FDA reports)
MORTON'S NEUROMA ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
NEURALGIA ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
RASH ( 8 FDA reports)
DELIRIUM ( 7 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
MASS ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
ANGER ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
FEAR ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OBESITY ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
RHEUMATIC HEART DISEASE ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POLYP ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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