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

PAIN ( 32 FDA reports)
NAUSEA ( 18 FDA reports)
ANXIETY ( 17 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
VOMITING ( 15 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
RENAL INJURY ( 14 FDA reports)
INJURY ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
ANHEDONIA ( 12 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DEATH ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
FALL ( 11 FDA reports)
STRESS ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
BONE PAIN ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
UNEVALUABLE EVENT ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
FEAR ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
SCAR ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HYPOTENSION ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
JOINT STIFFNESS ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
SKIN HYPERTROPHY ( 7 FDA reports)
SKIN TIGHTNESS ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SWELLING ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RASH ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DEFORMITY ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN FIBROSIS ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ANGER ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COMA ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
APHONIA ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
PSYCHOLOGICAL FACTOR AFFECTING MEDICAL CONDITION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN THRESHOLD DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use