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

PAIN ( 133 FDA reports)
ANXIETY ( 120 FDA reports)
NAUSEA ( 93 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 89 FDA reports)
OSTEOMYELITIS ( 80 FDA reports)
INJURY ( 79 FDA reports)
FALL ( 78 FDA reports)
DYSPNOEA ( 77 FDA reports)
FATIGUE ( 76 FDA reports)
DIZZINESS ( 75 FDA reports)
OSTEONECROSIS OF JAW ( 75 FDA reports)
HEADACHE ( 74 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 69 FDA reports)
ASTHENIA ( 67 FDA reports)
VOMITING ( 67 FDA reports)
HYPERTENSION ( 65 FDA reports)
DEPRESSION ( 64 FDA reports)
ABDOMINAL PAIN ( 63 FDA reports)
CARDIAC DISORDER ( 62 FDA reports)
NEUROPATHY PERIPHERAL ( 61 FDA reports)
ATRIAL FIBRILLATION ( 60 FDA reports)
CHEST PAIN ( 59 FDA reports)
DIARRHOEA ( 59 FDA reports)
PLEURAL EFFUSION ( 59 FDA reports)
BONE DISORDER ( 58 FDA reports)
HYPOAESTHESIA ( 58 FDA reports)
CONSTIPATION ( 57 FDA reports)
OSTEOARTHRITIS ( 56 FDA reports)
PAIN IN JAW ( 56 FDA reports)
ARTHRALGIA ( 55 FDA reports)
ANAEMIA ( 54 FDA reports)
PNEUMONIA ( 54 FDA reports)
WEIGHT DECREASED ( 53 FDA reports)
GASTRITIS ( 51 FDA reports)
OSTEOPENIA ( 51 FDA reports)
SINUSITIS ( 50 FDA reports)
TOOTH EXTRACTION ( 50 FDA reports)
BACK PAIN ( 49 FDA reports)
BONE DEBRIDEMENT ( 49 FDA reports)
DRUG INEFFECTIVE ( 48 FDA reports)
HYPOKALAEMIA ( 48 FDA reports)
ATELECTASIS ( 47 FDA reports)
PULMONARY OEDEMA ( 47 FDA reports)
CELLULITIS ( 44 FDA reports)
JAW FRACTURE ( 44 FDA reports)
PYREXIA ( 44 FDA reports)
CONFUSIONAL STATE ( 43 FDA reports)
OEDEMA PERIPHERAL ( 43 FDA reports)
CORONARY ARTERY DISEASE ( 42 FDA reports)
RENAL FAILURE CHRONIC ( 41 FDA reports)
CARDIOMEGALY ( 40 FDA reports)
DYSPHAGIA ( 40 FDA reports)
MUSCLE SPASMS ( 40 FDA reports)
SWELLING ( 40 FDA reports)
BURSITIS ( 39 FDA reports)
CATARACT ( 39 FDA reports)
ASTHMA ( 38 FDA reports)
JAW OPERATION ( 38 FDA reports)
HYPOTENSION ( 37 FDA reports)
MYOCARDIAL INFARCTION ( 37 FDA reports)
PULMONARY EMBOLISM ( 37 FDA reports)
SEPSIS ( 37 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 36 FDA reports)
VISION BLURRED ( 36 FDA reports)
BACK DISORDER ( 35 FDA reports)
DECREASED APPETITE ( 35 FDA reports)
IMPAIRED HEALING ( 35 FDA reports)
SPINAL OSTEOARTHRITIS ( 35 FDA reports)
VISUAL IMPAIRMENT ( 35 FDA reports)
WEIGHT INCREASED ( 35 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 34 FDA reports)
INFECTION ( 34 FDA reports)
INSOMNIA ( 34 FDA reports)
SWELLING FACE ( 34 FDA reports)
BRONCHITIS ( 33 FDA reports)
COUGH ( 33 FDA reports)
ABDOMINAL PAIN UPPER ( 32 FDA reports)
OSTEONECROSIS ( 32 FDA reports)
PARAESTHESIA ( 32 FDA reports)
ANHEDONIA ( 31 FDA reports)
RIB FRACTURE ( 31 FDA reports)
THROMBOCYTOPENIA ( 31 FDA reports)
CEREBROVASCULAR ACCIDENT ( 30 FDA reports)
DYSGEUSIA ( 30 FDA reports)
HYPERHIDROSIS ( 30 FDA reports)
HYPERKALAEMIA ( 30 FDA reports)
INFLAMMATION ( 30 FDA reports)
LYMPHADENOPATHY ( 30 FDA reports)
SPINAL COMPRESSION FRACTURE ( 30 FDA reports)
CONTUSION ( 29 FDA reports)
DYSPEPSIA ( 29 FDA reports)
BLOOD CALCIUM DECREASED ( 28 FDA reports)
BONE PAIN ( 28 FDA reports)
GAIT DISTURBANCE ( 28 FDA reports)
MASTICATION DISORDER ( 28 FDA reports)
MYALGIA ( 28 FDA reports)
ABSCESS ( 27 FDA reports)
BONE MARROW TRANSPLANT ( 27 FDA reports)
EMOTIONAL DISTRESS ( 27 FDA reports)
PAIN IN EXTREMITY ( 27 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 27 FDA reports)
MUSCULOSKELETAL PAIN ( 26 FDA reports)
OSTEOLYSIS ( 26 FDA reports)
SPINAL DISORDER ( 26 FDA reports)
TREMOR ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
CARDIAC ARREST ( 25 FDA reports)
DIABETES MELLITUS ( 25 FDA reports)
DRUG DEPENDENCE ( 25 FDA reports)
JOINT DISLOCATION ( 25 FDA reports)
PULMONARY CONGESTION ( 25 FDA reports)
RENAL FAILURE ( 25 FDA reports)
URINARY TRACT INFECTION ( 25 FDA reports)
CARDIOVASCULAR DISORDER ( 24 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 24 FDA reports)
COAGULOPATHY ( 24 FDA reports)
COLON CANCER ( 24 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 24 FDA reports)
FACE OEDEMA ( 24 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 24 FDA reports)
NECK PAIN ( 24 FDA reports)
RESPIRATORY FAILURE ( 24 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 24 FDA reports)
DECREASED INTEREST ( 23 FDA reports)
EJECTION FRACTION DECREASED ( 23 FDA reports)
JOINT CREPITATION ( 23 FDA reports)
MITRAL VALVE CALCIFICATION ( 23 FDA reports)
NEPHROLITHIASIS ( 23 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 23 FDA reports)
ABSCESS JAW ( 22 FDA reports)
BIOPSY BONE ABNORMAL ( 22 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 22 FDA reports)
DENTAL FISTULA ( 22 FDA reports)
EDENTULOUS ( 22 FDA reports)
ENCEPHALOPATHY ( 22 FDA reports)
GINGIVAL INFECTION ( 22 FDA reports)
HYPOXIA ( 22 FDA reports)
MACROGLOSSIA ( 22 FDA reports)
MALNUTRITION ( 22 FDA reports)
MASS ( 22 FDA reports)
MITRAL VALVE INCOMPETENCE ( 22 FDA reports)
NERVOUSNESS ( 22 FDA reports)
OSTEOPOROSIS ( 22 FDA reports)
OSTEOSCLEROSIS ( 22 FDA reports)
PERIODONTAL DISEASE ( 22 FDA reports)
PHYSICAL DISABILITY ( 22 FDA reports)
RASH ( 22 FDA reports)
SICK SINUS SYNDROME ( 22 FDA reports)
SOFT TISSUE DISORDER ( 22 FDA reports)
SPEECH DISORDER ( 22 FDA reports)
TONGUE ULCERATION ( 22 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
X-RAY ABNORMAL ( 22 FDA reports)
BRUXISM ( 21 FDA reports)
CHARLES BONNET SYNDROME ( 21 FDA reports)
DEAFNESS NEUROSENSORY ( 21 FDA reports)
DENTAL CARIES ( 21 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 21 FDA reports)
HIATUS HERNIA ( 21 FDA reports)
INTRACRANIAL ANEURYSM ( 21 FDA reports)
KLEBSIELLA INFECTION ( 21 FDA reports)
PSEUDOMONAS INFECTION ( 21 FDA reports)
SINUS DISORDER ( 21 FDA reports)
SUICIDAL IDEATION ( 21 FDA reports)
TREATMENT NONCOMPLIANCE ( 21 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
CATHETERISATION CARDIAC ( 20 FDA reports)
DISABILITY ( 20 FDA reports)
GINGIVAL PAIN ( 20 FDA reports)
MULTIPLE SCLEROSIS ( 20 FDA reports)
PURULENT DISCHARGE ( 20 FDA reports)
SPINAL COLUMN STENOSIS ( 20 FDA reports)
THROMBOSIS IN DEVICE ( 20 FDA reports)
DEATH ( 19 FDA reports)
DEVICE FAILURE ( 19 FDA reports)
ENDOTRACHEAL INTUBATION ( 19 FDA reports)
FACIAL PAIN ( 19 FDA reports)
HEPATIC STEATOSIS ( 19 FDA reports)
IRRITABILITY ( 19 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 19 FDA reports)
SEQUESTRECTOMY ( 19 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 18 FDA reports)
ANGINA PECTORIS ( 18 FDA reports)
ARTHROPATHY ( 18 FDA reports)
BLINDNESS ( 18 FDA reports)
CARDIAC PACEMAKER INSERTION ( 18 FDA reports)
CHOLECYSTECTOMY ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
DEAFNESS ( 18 FDA reports)
DILATATION VENTRICULAR ( 18 FDA reports)
EAR NEOPLASM ( 18 FDA reports)
FANCONI SYNDROME ( 18 FDA reports)
GALLBLADDER DISORDER ( 18 FDA reports)
GINGIVAL SWELLING ( 18 FDA reports)
GRANULOMA ( 18 FDA reports)
HIP FRACTURE ( 18 FDA reports)
HYDROCEPHALUS ( 18 FDA reports)
MOUTH ULCERATION ( 18 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 18 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 18 FDA reports)
PULMONARY HYPERTENSION ( 18 FDA reports)
SKIN LACERATION ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ADDISON'S DISEASE ( 17 FDA reports)
AMNESIA ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
COLECTOMY ( 17 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 17 FDA reports)
EXTREMITY NECROSIS ( 17 FDA reports)
FISTULA REPAIR ( 17 FDA reports)
GINGIVAL ULCERATION ( 17 FDA reports)
GINGIVITIS ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
HYPERPARATHYROIDISM ( 17 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 17 FDA reports)
KYPHOSCOLIOSIS ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
MYOCLONUS ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 17 FDA reports)
PLEURAL FIBROSIS ( 17 FDA reports)
RENAL DISORDER ( 17 FDA reports)
SEPTIC SHOCK ( 17 FDA reports)
SINUS OPERATION ( 17 FDA reports)
STREPTOCOCCAL SEPSIS ( 17 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
HYPOTHYROIDISM ( 16 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 16 FDA reports)
JOINT INJURY ( 16 FDA reports)
MALAISE ( 16 FDA reports)
MECHANICAL VENTILATION ( 16 FDA reports)
METASTASES TO SPINE ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 16 FDA reports)
PATHOLOGICAL FRACTURE ( 16 FDA reports)
PROTEIN URINE PRESENT ( 16 FDA reports)
SARCOIDOSIS ( 16 FDA reports)
STRESS ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
VENA CAVA FILTER INSERTION ( 16 FDA reports)
BONE LESION ( 15 FDA reports)
BURNING SENSATION ( 15 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 15 FDA reports)
FEMUR FRACTURE ( 15 FDA reports)
HAEMATURIA ( 15 FDA reports)
HYPERLIPIDAEMIA ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
MUCOSAL INFLAMMATION ( 15 FDA reports)
MYELOMA RECURRENCE ( 15 FDA reports)
MYOCARDIAL ISCHAEMIA ( 15 FDA reports)
NASOPHARYNGITIS ( 15 FDA reports)
ORAL INFECTION ( 15 FDA reports)
OSTEITIS ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
POLYP ( 15 FDA reports)
ROTATOR CUFF SYNDROME ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
SYNOVIAL CYST ( 15 FDA reports)
UTERINE LEIOMYOMA ( 15 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ALKALOSIS ( 14 FDA reports)
APLASTIC ANAEMIA ( 14 FDA reports)
CHILLS ( 14 FDA reports)
COLONIC POLYP ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
ECONOMIC PROBLEM ( 14 FDA reports)
FIBROMA ( 14 FDA reports)
HAEMATOCHEZIA ( 14 FDA reports)
ORTHOSTATIC HYPOTENSION ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
PULMONARY ARTERY DILATATION ( 14 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
SQUAMOUS CELL CARCINOMA ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 13 FDA reports)
ARRHYTHMIA ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CHEST DISCOMFORT ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
DRUG ABUSER ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
HYPERSENSITIVITY ( 13 FDA reports)
HYSTERECTOMY ( 13 FDA reports)
MEMORY IMPAIRMENT ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 13 FDA reports)
OEDEMA MOUTH ( 13 FDA reports)
ORAL CAVITY FISTULA ( 13 FDA reports)
PANCREATIC CYST ( 13 FDA reports)
PRURITUS ( 13 FDA reports)
ROAD TRAFFIC ACCIDENT ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
ARTERIOSCLEROSIS ( 12 FDA reports)
BACTERIAL DISEASE CARRIER ( 12 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 12 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 12 FDA reports)
BLEPHARITIS ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
CARBON DIOXIDE INCREASED ( 12 FDA reports)
CORONARY ARTERY BYPASS ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
ENDODONTIC PROCEDURE ( 12 FDA reports)
ERECTILE DYSFUNCTION ( 12 FDA reports)
FEAR ( 12 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 12 FDA reports)
JOINT SURGERY ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
LUNG DISORDER ( 12 FDA reports)
MANDIBULAR PROSTHESIS USER ( 12 FDA reports)
MITRAL VALVE REPLACEMENT ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
NASAL CONGESTION ( 12 FDA reports)
OTITIS MEDIA CHRONIC ( 12 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SKIN LESION ( 12 FDA reports)
THERMAL BURN ( 12 FDA reports)
TRACHEOSTOMY ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
WOUND DRAINAGE ( 12 FDA reports)
ADRENAL INSUFFICIENCY ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
HEART RATE INCREASED ( 11 FDA reports)
ILEUS ( 11 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
LACERATION ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NIGHT SWEATS ( 11 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 11 FDA reports)
PRODUCTIVE COUGH ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
RESTLESS LEGS SYNDROME ( 11 FDA reports)
ANGINA UNSTABLE ( 10 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
CRYING ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
GASTRIC DISORDER ( 10 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPERTHYROIDISM ( 10 FDA reports)
IRRITABLE BOWEL SYNDROME ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
LOW TURNOVER OSTEOPATHY ( 10 FDA reports)
LUNG INFILTRATION ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
OFF LABEL USE ( 10 FDA reports)
RENAL INJURY ( 10 FDA reports)
STEM CELL TRANSPLANT ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
THROMBECTOMY ( 10 FDA reports)
ULCER ( 10 FDA reports)
VENTRICULAR HYPERTROPHY ( 10 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
AFFECTIVE DISORDER ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
ARTHRITIS ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 9 FDA reports)
DEMENTIA ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
FOOT FRACTURE ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
HEAD INJURY ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LUMBAR RADICULOPATHY ( 9 FDA reports)
LUMBAR SPINAL STENOSIS ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
PANCREATECTOMY ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
POLLAKIURIA ( 9 FDA reports)
RECTAL HAEMORRHAGE ( 9 FDA reports)
SKIN ATROPHY ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SPLENECTOMY ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ADVERSE DRUG REACTION ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BRONCHITIS ACUTE ( 8 FDA reports)
CONJUNCTIVITIS ( 8 FDA reports)
DRUG SCREEN POSITIVE ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
GYNAECOMASTIA ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
IRON DEFICIENCY ( 8 FDA reports)
LIGAMENT SPRAIN ( 8 FDA reports)
NEOPLASM ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PYELONEPHRITIS ( 8 FDA reports)
SELF ESTEEM DECREASED ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TENSION ( 8 FDA reports)
TUMOUR NECROSIS ( 8 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 8 FDA reports)
VIRAL INFECTION ( 8 FDA reports)
ANGIOPLASTY ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
APPENDICITIS ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
CARDIAC OPERATION ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
CYST ( 7 FDA reports)
DERMATITIS CONTACT ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
HYPOVOLAEMIA ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LIMB OPERATION ( 7 FDA reports)
LIP SWELLING ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
NEURODERMATITIS ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
ORAL SURGERY ( 7 FDA reports)
PAIN EXACERBATED ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PRESCRIBED OVERDOSE ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TRIGGER FINGER ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
ALVEOLOPLASTY ( 6 FDA reports)
ANEURYSM ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BINGE EATING ( 6 FDA reports)
BLISTER ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
CARPAL TUNNEL SYNDROME ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
CUTANEOUS VASCULITIS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
NASAL SEPTUM DEVIATION ( 6 FDA reports)
OBESITY ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
PYODERMA ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SKIN GRAFT FAILURE ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
TOOTH INFECTION ( 6 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
URETHRAL STRICTURE ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
WOUND ( 6 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BREAST HAEMATOMA ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COLON CANCER STAGE IV ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DEFORMITY ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HUNGER ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
METAPLASIA ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VITREOUS FLOATERS ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEGAL PROBLEM ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCULAR DYSTROPHY ( 4 FDA reports)
NASAL OBSTRUCTION ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OSTEORADIONECROSIS ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SECONDARY SEQUESTRUM ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC CANCER RECURRENT ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCROTAL CYST ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EAR TUBE REMOVAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERINSULINISM ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOTONSILLECTOMY ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGOSCOPY ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGOTOMY ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)

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