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

DYSPNOEA ( 103 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 96 FDA reports)
HEADACHE ( 71 FDA reports)
FATIGUE ( 66 FDA reports)
VISUAL ACUITY REDUCED ( 65 FDA reports)
VISION BLURRED ( 60 FDA reports)
PAIN ( 53 FDA reports)
CATARACT ( 52 FDA reports)
DIZZINESS ( 52 FDA reports)
ARTHRALGIA ( 50 FDA reports)
ASTHENIA ( 50 FDA reports)
GLAUCOMA ( 50 FDA reports)
COUGH ( 44 FDA reports)
DEHYDRATION ( 44 FDA reports)
VOMITING ( 44 FDA reports)
EYE IRRITATION ( 43 FDA reports)
OCULAR HYPERAEMIA ( 43 FDA reports)
DRUG INEFFECTIVE ( 41 FDA reports)
OEDEMA PERIPHERAL ( 41 FDA reports)
FALL ( 40 FDA reports)
EYE PAIN ( 39 FDA reports)
CONDITION AGGRAVATED ( 37 FDA reports)
PAIN IN EXTREMITY ( 37 FDA reports)
DEPRESSION ( 36 FDA reports)
NAUSEA ( 35 FDA reports)
ABDOMINAL PAIN ( 33 FDA reports)
ANAEMIA ( 32 FDA reports)
DIARRHOEA ( 31 FDA reports)
HYPERTENSION ( 31 FDA reports)
VISUAL IMPAIRMENT ( 30 FDA reports)
PRURITUS ( 29 FDA reports)
ANXIETY ( 28 FDA reports)
GAIT DISTURBANCE ( 28 FDA reports)
RENAL FAILURE ( 27 FDA reports)
URINARY TRACT INFECTION ( 27 FDA reports)
CONSTIPATION ( 26 FDA reports)
NEUTROPENIA ( 26 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
ASTHMA ( 25 FDA reports)
BLOOD CREATININE INCREASED ( 25 FDA reports)
BRADYCARDIA ( 25 FDA reports)
CELLULITIS ( 25 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 25 FDA reports)
BACK PAIN ( 24 FDA reports)
INJURY ( 24 FDA reports)
MYALGIA ( 24 FDA reports)
RASH ( 24 FDA reports)
HYPERSENSITIVITY ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
INFECTION ( 23 FDA reports)
LYMPHADENOPATHY ( 23 FDA reports)
PNEUMONIA ( 23 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
ARRHYTHMIA ( 22 FDA reports)
EYE DISORDER ( 22 FDA reports)
MALNUTRITION ( 22 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
PLEURAL EFFUSION ( 22 FDA reports)
SCAR ( 22 FDA reports)
ATELECTASIS ( 21 FDA reports)
EYELID OEDEMA ( 21 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 20 FDA reports)
CONFUSIONAL STATE ( 20 FDA reports)
EYE PRURITUS ( 20 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 20 FDA reports)
INSOMNIA ( 20 FDA reports)
PALPITATIONS ( 20 FDA reports)
PYREXIA ( 20 FDA reports)
VISUAL FIELD DEFECT ( 20 FDA reports)
BALANCE DISORDER ( 19 FDA reports)
BLOOD UREA INCREASED ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 19 FDA reports)
CHILLS ( 19 FDA reports)
EMOTIONAL DISTRESS ( 19 FDA reports)
HAEMATURIA ( 19 FDA reports)
MALAISE ( 19 FDA reports)
METASTASES TO BONE ( 19 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
BLOOD GLUCOSE INCREASED ( 18 FDA reports)
COLLAPSE OF LUNG ( 18 FDA reports)
DRY MOUTH ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
HEART RATE IRREGULAR ( 18 FDA reports)
MENTAL STATUS CHANGES ( 18 FDA reports)
PHYSICAL DISABILITY ( 18 FDA reports)
BACTERIAL INFECTION ( 17 FDA reports)
CHOLELITHIASIS ( 17 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
EPISTAXIS ( 17 FDA reports)
LACRIMATION INCREASED ( 17 FDA reports)
TACHYCARDIA ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
HYPERHIDROSIS ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
OSTEOPENIA ( 16 FDA reports)
OSTEOPOROSIS ( 16 FDA reports)
ABDOMINAL DISCOMFORT ( 15 FDA reports)
ABNORMAL SENSATION IN EYE ( 15 FDA reports)
ALOPECIA ( 15 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 15 FDA reports)
CONTUSION ( 15 FDA reports)
DYSURIA ( 15 FDA reports)
ENDOPHTHALMITIS ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
LEUKOPENIA ( 15 FDA reports)
METASTASES TO LIVER ( 15 FDA reports)
METASTASES TO SPINE ( 15 FDA reports)
METASTASES TO THORAX ( 15 FDA reports)
NECK PAIN ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
STRESS FRACTURE ( 15 FDA reports)
TENDON DISORDER ( 15 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLINDNESS ( 14 FDA reports)
BONE LESION ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
BONE PAIN ( 14 FDA reports)
CARCINOID SYNDROME ( 14 FDA reports)
CARDIAC DISORDER ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CORNEAL DISORDER ( 14 FDA reports)
DYSKINESIA ( 14 FDA reports)
DYSPEPSIA ( 14 FDA reports)
EFFUSION ( 14 FDA reports)
ENTHESOPATHY ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
PLANTAR FASCIITIS ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
SYNOVIAL CYST ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
BLINDNESS UNILATERAL ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
DEAFNESS ( 13 FDA reports)
DRUG HYPERSENSITIVITY ( 13 FDA reports)
DYSPHAGIA ( 13 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 13 FDA reports)
OSTEOSCLEROSIS ( 13 FDA reports)
PULMONARY GRANULOMA ( 13 FDA reports)
VENOUS OCCLUSION ( 13 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 12 FDA reports)
INJECTION SITE PAIN ( 12 FDA reports)
INTESTINAL RESECTION ( 12 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 12 FDA reports)
PYELONEPHRITIS ACUTE ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
SINUSITIS ( 12 FDA reports)
AMNESIA ( 11 FDA reports)
CORNEAL EROSION ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
DRY EYE ( 11 FDA reports)
DYSGEUSIA ( 11 FDA reports)
EYE DISCHARGE ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
LUNG CONSOLIDATION ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
STREPTOCOCCAL INFECTION ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 10 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 10 FDA reports)
TREMOR ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
FRACTURED SACRUM ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HEPATIC LESION ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
JUVENILE ARTHRITIS ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
NEUROENDOCRINE TUMOUR ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
PHOTOPHOBIA ( 9 FDA reports)
PUNCTATE KERATITIS ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
WEGENER'S GRANULOMATOSIS ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 8 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
EYE OPERATION ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
KERATITIS ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
OCULAR HYPERTENSION ( 8 FDA reports)
OPTIC ATROPHY ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
CHOLANGITIS ( 7 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 7 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
DEATH ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ERYTHEMA OF EYELID ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FEAR ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
GROWTH OF EYELASHES ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
METASTATIC CARCINOID TUMOUR ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
NIGHT BLINDNESS ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
SPINAL FRACTURE ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
UVEITIS ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CATARACT OPERATION ( 6 FDA reports)
CONJUNCTIVAL OEDEMA ( 6 FDA reports)
CORNEAL OEDEMA ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DYSPLASIA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
IRITIS ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEAFNESS TRANSITORY ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
MACULAR HOLE ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANTERIOR CHAMBER CELL ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CATARACT CORTICAL ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHOROIDAL DETACHMENT ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CRYING ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
ERYTHEMA ANNULARE ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
POLYPECTOMY ( 4 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SOPOR ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
WAGNER'S DISEASE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
APATHY ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COCCYDYNIA ( 3 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
ENOPHTHALMOS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EYE INFECTION BACTERIAL ( 3 FDA reports)
EYELASH THICKENING ( 3 FDA reports)
EYELID IRRITATION ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GLAUCOMA SURGERY ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOTONY OF EYE ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
OROPHARYNGEAL SPASM ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
RHEUMATOID FACTOR NEGATIVE ( 3 FDA reports)
SCLERAL DISORDER ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTO-DUODENAL FISTULA ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLEPHARAL PIGMENTATION ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BUNION ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEREBELLAR TUMOUR ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL SCAR ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FRACTURE TREATMENT ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRIS HYPERPIGMENTATION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KERATORHEXIS ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT MELANOMA OF EYELID ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PINEAL NEOPLASM ( 2 FDA reports)
POLYDACTYLY ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUDDEN VISUAL LOSS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRABECULECTOMY ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACOUSTIC NEURITIS ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DECREASED ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS PASTEURELLA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL GRANULOMA ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DESCEMET'S MEMBRANE DISORDER ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEREDITARY DISORDER ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE OPERATION ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMATOFORM DISORDER NEUROLOGIC ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use