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

DIARRHOEA ( 30 FDA reports)
ANAEMIA ( 28 FDA reports)
PAIN ( 28 FDA reports)
DYSPNOEA ( 25 FDA reports)
ANXIETY ( 20 FDA reports)
PULMONARY EMBOLISM ( 19 FDA reports)
CHEST PAIN ( 18 FDA reports)
INJURY ( 18 FDA reports)
DEEP VEIN THROMBOSIS ( 17 FDA reports)
OSTEONECROSIS OF JAW ( 17 FDA reports)
NAUSEA ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
VOMITING ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
ATELECTASIS ( 14 FDA reports)
FALL ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
ARTHRALGIA ( 12 FDA reports)
ATRIAL SEPTAL DEFECT ( 12 FDA reports)
CHOLESTASIS ( 12 FDA reports)
GAIT DISTURBANCE ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
HIATUS HERNIA ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
RESPIRATORY DISTRESS ( 12 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
EMOTIONAL DISTRESS ( 11 FDA reports)
SPINAL OSTEOARTHRITIS ( 11 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
MALAISE ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HAEMORRHOIDS ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
OSTEOMYELITIS ( 9 FDA reports)
RASH ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
ANHEDONIA ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
DEFORMITY ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
TOOTH ABSCESS ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PLEURAL FIBROSIS ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DEXTROCARDIA ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OSTEOLYSIS ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PARAPROTEINAEMIA ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GINGIVAL SWELLING ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NASAL SEPTUM DEVIATION ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SNORING ( 4 FDA reports)
SPLENIC LESION ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABSCESS JAW ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLESTEATOMA ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
KYPHOSCOLIOSIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METATARSUS PRIMUS VARUS ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS SEASONAL ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASAL VESTIBULITIS ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use