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

BLOOD GLUCOSE INCREASED ( 115 FDA reports)
NAUSEA ( 103 FDA reports)
WEIGHT DECREASED ( 86 FDA reports)
FLUSHING ( 60 FDA reports)
DIZZINESS ( 51 FDA reports)
BLOOD GLUCOSE DECREASED ( 48 FDA reports)
ASTHENIA ( 47 FDA reports)
DYSPNOEA ( 47 FDA reports)
BLADDER CANCER ( 39 FDA reports)
DECREASED APPETITE ( 38 FDA reports)
VOMITING ( 37 FDA reports)
OEDEMA PERIPHERAL ( 33 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
CHEST PAIN ( 32 FDA reports)
FATIGUE ( 32 FDA reports)
ABDOMINAL PAIN UPPER ( 31 FDA reports)
BACK PAIN ( 30 FDA reports)
HEADACHE ( 30 FDA reports)
WEIGHT INCREASED ( 30 FDA reports)
MYALGIA ( 28 FDA reports)
PRURITUS ( 28 FDA reports)
PAIN ( 27 FDA reports)
URINARY TRACT INFECTION ( 27 FDA reports)
ANXIETY ( 26 FDA reports)
RASH ( 26 FDA reports)
ARTHRALGIA ( 25 FDA reports)
DRUG INEFFECTIVE ( 25 FDA reports)
FALL ( 25 FDA reports)
FEELING HOT ( 25 FDA reports)
TREMOR ( 25 FDA reports)
DIARRHOEA ( 24 FDA reports)
MALAISE ( 23 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
SOMNOLENCE ( 22 FDA reports)
ERYTHEMA ( 21 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
MUSCLE SPASMS ( 21 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
DEHYDRATION ( 19 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
GASTRITIS ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
INJECTION SITE HAEMORRHAGE ( 18 FDA reports)
PANCREATITIS ( 18 FDA reports)
URTICARIA ( 18 FDA reports)
ASTHMA ( 17 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 17 FDA reports)
INJECTION SITE BRUISING ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
SWELLING ( 17 FDA reports)
DEPRESSION ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
PARAESTHESIA ( 16 FDA reports)
CHILLS ( 15 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
ORAL CANDIDIASIS ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
DYSPEPSIA ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
INJURY ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
LETHARGY ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
ATELECTASIS ( 13 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
HYPERSOMNIA ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
IMPAIRED HEALING ( 12 FDA reports)
INJECTION SITE PAIN ( 12 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
TYPE 2 DIABETES MELLITUS ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CARDIAC MURMUR ( 11 FDA reports)
COUGH ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
HYPERLIPIDAEMIA ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
OSTEOPENIA ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
SYNCOPE ( 11 FDA reports)
DEATH ( 10 FDA reports)
DRUG EFFECT DECREASED ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
OSTEOARTHRITIS ( 10 FDA reports)
RENAL DISORDER ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
BRONCHITIS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DERMAL CYST ( 9 FDA reports)
GALLBLADDER DISORDER ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
ARTHROPATHY ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
EPIGASTRIC DISCOMFORT ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MULTIPLE MYELOMA ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SUPERINFECTION ( 8 FDA reports)
TOBACCO ABUSE ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 7 FDA reports)
ADRENAL SUPPRESSION ( 7 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 7 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
ARTHRITIS BACTERIAL ( 7 FDA reports)
BACTERIAL DIARRHOEA ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BONE LESION ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
BULLOUS LUNG DISEASE ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
DECREASED INTEREST ( 7 FDA reports)
DYSLIPIDAEMIA ( 7 FDA reports)
DYSPHEMIA ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
ERUCTATION ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMORRHOIDS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
INFECTIVE TENOSYNOVITIS ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
LUMBAR SPINAL STENOSIS ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NERVE ROOT COMPRESSION ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
OSTEITIS ( 7 FDA reports)
OSTEOLYSIS ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
PELVIC FRACTURE ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PNEUMONITIS ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
STREPTOCOCCAL SEPSIS ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
VASCULAR CALCIFICATION ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
ABASIA ( 6 FDA reports)
APHASIA ( 6 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CAUDA EQUINA SYNDROME ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RETCHING ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SNORING ( 6 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANGER ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
HUNGER ( 5 FDA reports)
IRITIS ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
MELANOSIS COLI ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RECTAL POLYP ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
STRESS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CHOLESTEROSIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EARLY SATIETY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL OBSTRUCTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL VENOUS GAS ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS ULCERATIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO URINARY TRACT ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDIAL STRAIN ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS CHEMICAL ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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