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

DIZZINESS ( 258 FDA reports)
PAIN ( 192 FDA reports)
ANXIETY ( 151 FDA reports)
ASTHENIA ( 148 FDA reports)
NAUSEA ( 137 FDA reports)
DYSPNOEA ( 136 FDA reports)
FATIGUE ( 122 FDA reports)
URINARY TRACT INFECTION ( 121 FDA reports)
CHEST PAIN ( 120 FDA reports)
BACK PAIN ( 119 FDA reports)
FALL ( 116 FDA reports)
CEREBROVASCULAR ACCIDENT ( 112 FDA reports)
HEADACHE ( 111 FDA reports)
PAIN IN EXTREMITY ( 103 FDA reports)
VERTIGO ( 100 FDA reports)
ARTHRALGIA ( 96 FDA reports)
HYPERTENSION ( 95 FDA reports)
ANAEMIA ( 89 FDA reports)
DEPRESSION ( 89 FDA reports)
DIARRHOEA ( 89 FDA reports)
OEDEMA PERIPHERAL ( 83 FDA reports)
HYPOAESTHESIA ( 79 FDA reports)
VOMITING ( 77 FDA reports)
PYREXIA ( 73 FDA reports)
DEHYDRATION ( 70 FDA reports)
OSTEOMYELITIS ( 68 FDA reports)
PNEUMONIA ( 68 FDA reports)
WEIGHT DECREASED ( 68 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 67 FDA reports)
VISION BLURRED ( 67 FDA reports)
DRUG INEFFECTIVE ( 66 FDA reports)
PALPITATIONS ( 66 FDA reports)
EMOTIONAL DISTRESS ( 65 FDA reports)
GAIT DISTURBANCE ( 65 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 65 FDA reports)
INJURY ( 64 FDA reports)
INSOMNIA ( 64 FDA reports)
MUSCLE SPASMS ( 64 FDA reports)
COUGH ( 62 FDA reports)
CATARACT ( 59 FDA reports)
OSTEOARTHRITIS ( 59 FDA reports)
ATRIAL FIBRILLATION ( 58 FDA reports)
NEUROPATHY PERIPHERAL ( 57 FDA reports)
ABDOMINAL PAIN ( 56 FDA reports)
CELLULITIS ( 55 FDA reports)
OSTEONECROSIS OF JAW ( 52 FDA reports)
RASH ( 50 FDA reports)
CHILLS ( 48 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 48 FDA reports)
DENTAL CARIES ( 48 FDA reports)
PARAESTHESIA ( 48 FDA reports)
FEELING ABNORMAL ( 46 FDA reports)
BLOOD GLUCOSE INCREASED ( 45 FDA reports)
CONFUSIONAL STATE ( 45 FDA reports)
DEATH ( 45 FDA reports)
DYSPHAGIA ( 45 FDA reports)
MALAISE ( 45 FDA reports)
ANGINA PECTORIS ( 44 FDA reports)
HYPERLIPIDAEMIA ( 44 FDA reports)
MEMORY IMPAIRMENT ( 44 FDA reports)
SEPSIS ( 44 FDA reports)
BLOOD PRESSURE INCREASED ( 43 FDA reports)
ECONOMIC PROBLEM ( 43 FDA reports)
ARRHYTHMIA ( 42 FDA reports)
BALANCE DISORDER ( 42 FDA reports)
SOMNOLENCE ( 42 FDA reports)
AMNESIA ( 41 FDA reports)
CHOLELITHIASIS ( 41 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
HYPOTENSION ( 41 FDA reports)
MITRAL VALVE INCOMPETENCE ( 41 FDA reports)
TOOTH FRACTURE ( 41 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 41 FDA reports)
ASTHMA ( 40 FDA reports)
MYOCARDIAL INFARCTION ( 40 FDA reports)
URINARY RETENTION ( 39 FDA reports)
ERYTHEMA ( 38 FDA reports)
TREMOR ( 38 FDA reports)
BRONCHITIS ( 37 FDA reports)
CORONARY ARTERY DISEASE ( 37 FDA reports)
DECREASED APPETITE ( 37 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 37 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 37 FDA reports)
MUSCULOSKELETAL PAIN ( 37 FDA reports)
SPINAL OSTEOARTHRITIS ( 37 FDA reports)
BONE DISORDER ( 36 FDA reports)
CONTUSION ( 36 FDA reports)
MIGRAINE ( 36 FDA reports)
OVERDOSE ( 36 FDA reports)
SLEEP APNOEA SYNDROME ( 36 FDA reports)
AGITATION ( 35 FDA reports)
HAEMOGLOBIN DECREASED ( 35 FDA reports)
RENAL FAILURE ( 35 FDA reports)
RENAL FAILURE ACUTE ( 35 FDA reports)
SINUSITIS ( 35 FDA reports)
ABDOMINAL PAIN UPPER ( 34 FDA reports)
ATELECTASIS ( 34 FDA reports)
DIABETES MELLITUS ( 34 FDA reports)
NIGHT SWEATS ( 34 FDA reports)
PRESYNCOPE ( 34 FDA reports)
TACHYCARDIA ( 34 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 34 FDA reports)
ARTHRITIS ( 33 FDA reports)
CARDIAC DISORDER ( 33 FDA reports)
DIPLOPIA ( 33 FDA reports)
DYSPEPSIA ( 33 FDA reports)
LYMPHADENOPATHY ( 33 FDA reports)
CONSTIPATION ( 32 FDA reports)
ROTATOR CUFF SYNDROME ( 32 FDA reports)
DISORIENTATION ( 31 FDA reports)
MASTICATION DISORDER ( 31 FDA reports)
DYSURIA ( 30 FDA reports)
NECK PAIN ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
PRURITUS ( 30 FDA reports)
TOOTH LOSS ( 30 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 30 FDA reports)
ANHEDONIA ( 29 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 29 FDA reports)
MUSCULAR WEAKNESS ( 29 FDA reports)
NERVOUSNESS ( 29 FDA reports)
SWELLING ( 29 FDA reports)
CARDIOMEGALY ( 28 FDA reports)
EJECTION FRACTION DECREASED ( 28 FDA reports)
HYPERSENSITIVITY ( 28 FDA reports)
MYALGIA ( 28 FDA reports)
PULMONARY EMBOLISM ( 28 FDA reports)
TINNITUS ( 28 FDA reports)
WEIGHT INCREASED ( 28 FDA reports)
CHEST DISCOMFORT ( 27 FDA reports)
DISTURBANCE IN ATTENTION ( 27 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
KYPHOSIS ( 27 FDA reports)
LABYRINTHITIS ( 27 FDA reports)
OESOPHAGEAL ULCER ( 27 FDA reports)
OROPHARYNGEAL PAIN ( 27 FDA reports)
SPINAL COMPRESSION FRACTURE ( 27 FDA reports)
ARTERIOSCLEROSIS ( 26 FDA reports)
CARDIOMYOPATHY ( 26 FDA reports)
CEREBRAL ATROPHY ( 26 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 26 FDA reports)
HYPERCHOLESTEROLAEMIA ( 26 FDA reports)
LUNG NEOPLASM ( 26 FDA reports)
TOOTH EXTRACTION ( 26 FDA reports)
ARTHROPATHY ( 25 FDA reports)
DYSPNOEA EXERTIONAL ( 25 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
HEPATIC STEATOSIS ( 25 FDA reports)
MENTAL DISORDER ( 25 FDA reports)
VISUAL IMPAIRMENT ( 25 FDA reports)
ATAXIA ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
INFECTION ( 24 FDA reports)
OSTEOPENIA ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 24 FDA reports)
GASTRITIS ( 23 FDA reports)
IRRITABLE BOWEL SYNDROME ( 23 FDA reports)
LOSS OF CONSCIOUSNESS ( 23 FDA reports)
PANCYTOPENIA ( 23 FDA reports)
SYNCOPE ( 23 FDA reports)
DRY MOUTH ( 22 FDA reports)
EATING DISORDER ( 22 FDA reports)
INFLUENZA LIKE ILLNESS ( 22 FDA reports)
PLEURAL EFFUSION ( 22 FDA reports)
STRESS ( 22 FDA reports)
THROMBOSIS ( 22 FDA reports)
VENTRICULAR TACHYCARDIA ( 22 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 21 FDA reports)
BONE PAIN ( 21 FDA reports)
DECREASED INTEREST ( 21 FDA reports)
DRUG HYPERSENSITIVITY ( 21 FDA reports)
EPISTAXIS ( 21 FDA reports)
HIATUS HERNIA ( 21 FDA reports)
MENISCUS LESION ( 21 FDA reports)
PAIN OF SKIN ( 21 FDA reports)
RADICULOPATHY ( 21 FDA reports)
SINUS DISORDER ( 21 FDA reports)
VESTIBULAR DISORDER ( 21 FDA reports)
ABSCESS JAW ( 20 FDA reports)
CARDIAC MURMUR ( 20 FDA reports)
DYSARTHRIA ( 20 FDA reports)
HIP FRACTURE ( 20 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 20 FDA reports)
METASTASES TO BONE ( 20 FDA reports)
PSYCHOTIC DISORDER ( 20 FDA reports)
PULMONARY HYPERTENSION ( 20 FDA reports)
RECTAL HAEMORRHAGE ( 20 FDA reports)
VENTRICULAR HYPERTROPHY ( 20 FDA reports)
ANXIETY DISORDER ( 19 FDA reports)
BRADYCARDIA ( 19 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 19 FDA reports)
DIVERTICULUM ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
EYE PAIN ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
GASTROENTERITIS ( 19 FDA reports)
HAEMOPTYSIS ( 19 FDA reports)
HAEMORRHAGIC ANAEMIA ( 19 FDA reports)
HYPOKALAEMIA ( 19 FDA reports)
LUNG INFILTRATION ( 19 FDA reports)
MOOD SWINGS ( 19 FDA reports)
OESOPHAGITIS ( 19 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 19 FDA reports)
UNRESPONSIVE TO STIMULI ( 19 FDA reports)
APNOEA ( 18 FDA reports)
BILE DUCT STONE ( 18 FDA reports)
BLOOD UREA INCREASED ( 18 FDA reports)
CONDITION AGGRAVATED ( 18 FDA reports)
DERMATITIS ( 18 FDA reports)
DEVICE MALFUNCTION ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 18 FDA reports)
FISTULA ( 18 FDA reports)
HYPERTENSIVE HEART DISEASE ( 18 FDA reports)
IMPAIRED HEALING ( 18 FDA reports)
INFLAMMATION ( 18 FDA reports)
INNER EAR DISORDER ( 18 FDA reports)
LEFT ATRIAL DILATATION ( 18 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 18 FDA reports)
MACULAR DEGENERATION ( 18 FDA reports)
MULTIPLE MYELOMA ( 18 FDA reports)
MYOPATHY ( 18 FDA reports)
ORAL PAIN ( 18 FDA reports)
OSTEOSCLEROSIS ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
TESTICULAR PAIN ( 18 FDA reports)
WOUND ( 18 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 17 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 17 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 17 FDA reports)
BRONCHITIS CHRONIC ( 17 FDA reports)
CHOLECYSTITIS CHRONIC ( 17 FDA reports)
DEEP VEIN THROMBOSIS ( 17 FDA reports)
DEFORMITY ( 17 FDA reports)
DUODENITIS ( 17 FDA reports)
EYELID PTOSIS ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
HEART RATE IRREGULAR ( 17 FDA reports)
ILEUS ( 17 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 17 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 17 FDA reports)
MYOCARDIAL ISCHAEMIA ( 17 FDA reports)
NIGHTMARE ( 17 FDA reports)
NYSTAGMUS ( 17 FDA reports)
PHOTOPHOBIA ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
STAPHYLOCOCCAL INFECTION ( 17 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 17 FDA reports)
BLINDNESS UNILATERAL ( 16 FDA reports)
BLOOD CREATININE INCREASED ( 16 FDA reports)
BRONCHIAL SECRETION RETENTION ( 16 FDA reports)
CERVICAL CORD COMPRESSION ( 16 FDA reports)
CHONDROMALACIA ( 16 FDA reports)
COLONIC POLYP ( 16 FDA reports)
DENTAL PULP DISORDER ( 16 FDA reports)
EMOTIONAL DISORDER ( 16 FDA reports)
HAEMATOCHEZIA ( 16 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 16 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 16 FDA reports)
JOINT SWELLING ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
MENTAL STATUS CHANGES ( 16 FDA reports)
MYASTHENIA GRAVIS ( 16 FDA reports)
MYELODYSPLASTIC SYNDROME ( 16 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 16 FDA reports)
NEUTROPENIC SEPSIS ( 16 FDA reports)
PHONOPHOBIA ( 16 FDA reports)
PURULENCE ( 16 FDA reports)
SPINAL FUSION ACQUIRED ( 16 FDA reports)
SPUTUM DISCOLOURED ( 16 FDA reports)
SUBCUTANEOUS NODULE ( 16 FDA reports)
TENDERNESS ( 16 FDA reports)
TREATMENT NONCOMPLIANCE ( 16 FDA reports)
VENOUS THROMBOSIS ( 16 FDA reports)
ABDOMINAL DISCOMFORT ( 15 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BASAL CELL CARCINOMA ( 15 FDA reports)
CHROMATURIA ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
EAR PAIN ( 15 FDA reports)
FIBROMYALGIA ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
HERPES ZOSTER ( 15 FDA reports)
LETHARGY ( 15 FDA reports)
MULTIPLE INJURIES ( 15 FDA reports)
NEURITIS ( 15 FDA reports)
OESOPHAGEAL DISORDER ( 15 FDA reports)
OESOPHAGEAL STENOSIS ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
REFLUX OESOPHAGITIS ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
SCAR ( 15 FDA reports)
SKIN DISCOLOURATION ( 15 FDA reports)
SKIN ULCER ( 15 FDA reports)
SPEECH DISORDER ( 15 FDA reports)
SURGERY ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 14 FDA reports)
BONE DEBRIDEMENT ( 14 FDA reports)
BONE LOSS ( 14 FDA reports)
CAROTID ARTERY STENOSIS ( 14 FDA reports)
COLONOSCOPY ABNORMAL ( 14 FDA reports)
DIVERTICULITIS ( 14 FDA reports)
DRUG DEPENDENCE ( 14 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 14 FDA reports)
FLANK PAIN ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
GINGIVAL INFECTION ( 14 FDA reports)
GINGIVAL ULCERATION ( 14 FDA reports)
HAEMORRHAGE ( 14 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 14 FDA reports)
INCISIONAL DRAINAGE ( 14 FDA reports)
JOINT EFFUSION ( 14 FDA reports)
LACERATION ( 14 FDA reports)
MOBILITY DECREASED ( 14 FDA reports)
OBESITY ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 14 FDA reports)
SKIN HYPERTROPHY ( 14 FDA reports)
SKIN TIGHTNESS ( 14 FDA reports)
SOFT TISSUE INFECTION ( 14 FDA reports)
STASIS DERMATITIS ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
ACCIDENTAL OVERDOSE ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 13 FDA reports)
BURSITIS ( 13 FDA reports)
CATARACT OPERATION ( 13 FDA reports)
CONNECTIVE TISSUE DISORDER ( 13 FDA reports)
DISABILITY ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
DYSPHONIA ( 13 FDA reports)
EXCORIATION ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
INCONTINENCE ( 13 FDA reports)
JAUNDICE CHOLESTATIC ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
ORAL DISCOMFORT ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PRIMARY SEQUESTRUM ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
PULMONARY FIBROSIS ( 13 FDA reports)
RENAL CYST ( 13 FDA reports)
RHINORRHOEA ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
TOBACCO ABUSE ( 13 FDA reports)
TOOTH DISCOLOURATION ( 13 FDA reports)
ABASIA ( 12 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
ANEURYSM ( 12 FDA reports)
AORTIC VALVE STENOSIS ( 12 FDA reports)
BLOOD CALCIUM DECREASED ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
DYSKINESIA ( 12 FDA reports)
FEAR ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
ILL-DEFINED DISORDER ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
OEDEMA ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
ORAL DISCHARGE ( 12 FDA reports)
OTITIS MEDIA ( 12 FDA reports)
PLEURAL FIBROSIS ( 12 FDA reports)
PRODUCTIVE COUGH ( 12 FDA reports)
SEDATION ( 12 FDA reports)
SINUS BRADYCARDIA ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SKIN DISORDER ( 12 FDA reports)
SKIN LESION ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
TARDIVE DYSKINESIA ( 12 FDA reports)
VITAMIN D DEFICIENCY ( 12 FDA reports)
WHEEZING ( 12 FDA reports)
AORTIC VALVE INCOMPETENCE ( 11 FDA reports)
BARRETT'S OESOPHAGUS ( 11 FDA reports)
BURNING SENSATION ( 11 FDA reports)
CERUMEN IMPACTION ( 11 FDA reports)
COMA ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
HEART RATE DECREASED ( 11 FDA reports)
HYPOTHYROIDISM ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
NEURALGIA ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
PROSTATE CANCER ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 11 FDA reports)
SINUS CONGESTION ( 11 FDA reports)
SPINAL COLUMN STENOSIS ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
VARICOSE VEIN ( 11 FDA reports)
VENOUS INSUFFICIENCY ( 11 FDA reports)
ALOPECIA ( 10 FDA reports)
ASBESTOSIS ( 10 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 10 FDA reports)
BLOOD CREATININE DECREASED ( 10 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
COAGULOPATHY ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
DIABETES INSIPIDUS ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DRUG EFFECT DECREASED ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
GYNAECOMASTIA ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
SKIN HYPERPIGMENTATION ( 10 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 10 FDA reports)
TOOTHACHE ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 9 FDA reports)
BACK DISORDER ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
BODY TINEA ( 9 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 9 FDA reports)
COLITIS ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
CORONARY ARTERY STENOSIS ( 9 FDA reports)
DEVICE LEAKAGE ( 9 FDA reports)
DROP ATTACKS ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
HAEMANGIOMA ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
MITRAL VALVE PROLAPSE ( 9 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 9 FDA reports)
NASAL CONGESTION ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
RHEUMATOID ARTHRITIS ( 9 FDA reports)
SCOLIOSIS ( 9 FDA reports)
SLEEP DISORDER ( 9 FDA reports)
TINEA PEDIS ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TYPE 2 DIABETES MELLITUS ( 9 FDA reports)
URINARY HESITATION ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
CRYING ( 8 FDA reports)
CYST ( 8 FDA reports)
DERMATITIS ATOPIC ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DRUG INTOLERANCE ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
ERUCTATION ( 8 FDA reports)
ESSENTIAL HYPERTENSION ( 8 FDA reports)
EXPOSED BONE IN JAW ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
INTERTRIGO ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
NEPHROLITHIASIS ( 8 FDA reports)
NOCTURIA ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
PATHOLOGICAL GAMBLING ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RESTLESS LEGS SYNDROME ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
SCHAMBERG'S DISEASE ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
APHASIA ( 7 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
CERVICOBRACHIAL SYNDROME ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EPIDIDYMITIS ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
GALACTORRHOEA ( 7 FDA reports)
GENERAL SYMPTOM ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
JOINT STIFFNESS ( 7 FDA reports)
LABORATORY TEST ABNORMAL ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PRESCRIBED OVERDOSE ( 7 FDA reports)
PRODUCT QUALITY ISSUE ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SKIN BURNING SENSATION ( 7 FDA reports)
STRESS URINARY INCONTINENCE ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
THINKING ABNORMAL ( 7 FDA reports)
THIRST ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
VERTIGO POSITIONAL ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ANAL STENOSIS ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE ABNORMAL ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
COARCTATION OF THE AORTA ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DIZZINESS POSTURAL ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
ESSENTIAL TREMOR ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
FIBROSIS ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPERSOMNIA ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
KYPHOSCOLIOSIS ( 6 FDA reports)
LIGAMENT SPRAIN ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
LOOSE TOOTH ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 6 FDA reports)
PARAESTHESIA ORAL ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PYURIA ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
RHINITIS ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SARCOIDOSIS ( 6 FDA reports)
SERUM SICKNESS ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN DYSTROPHY ( 6 FDA reports)
SKIN FIBROSIS ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SNORING ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
CALCIUM DEFICIENCY ( 5 FDA reports)
CALCIUM IONISED INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GOUT ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MUSCLE STRAIN ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
TENDON INJURY ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
VIRAL LABYRINTHITIS ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ASCITES ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD PROLACTIN INCREASED ( 4 FDA reports)
BONE MARROW DISORDER ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COSTOCHONDRITIS ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN HYPOPIGMENTATION ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
ULCER ( 4 FDA reports)
ULNA FRACTURE ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ANGER ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
BLADDER DILATATION ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHOKING ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DENTURE WEARER ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FOREIGN BODY REACTION ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART INJURY ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INTERCEPTED MEDICATION ERROR ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OSTEORADIONECROSIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VOCAL CORD THICKENING ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLAST CELLS ABSENT ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLEFT UVULA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HETEROPHORIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MASS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTECTOMY ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETROGRADE EJACULATION ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALIVARY GLAND OPERATION ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMYLASE DECREASED ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL PROLAPSE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use