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

HYPERTENSION ( 42 FDA reports)
PAIN ( 41 FDA reports)
EYE PAIN ( 39 FDA reports)
ANXIETY ( 38 FDA reports)
VISUAL ACUITY REDUCED ( 38 FDA reports)
NAUSEA ( 31 FDA reports)
ULCERATIVE KERATITIS ( 31 FDA reports)
DIZZINESS ( 30 FDA reports)
FALL ( 30 FDA reports)
VOMITING ( 27 FDA reports)
BLINDNESS UNILATERAL ( 26 FDA reports)
CHEST PAIN ( 26 FDA reports)
DYSPNOEA ( 26 FDA reports)
VISION BLURRED ( 26 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 25 FDA reports)
ATRIAL FIBRILLATION ( 24 FDA reports)
FATIGUE ( 24 FDA reports)
HEADACHE ( 23 FDA reports)
ASTHENIA ( 22 FDA reports)
CATARACT ( 22 FDA reports)
ECONOMIC PROBLEM ( 22 FDA reports)
EYE IRRITATION ( 22 FDA reports)
BLOOD GLUCOSE INCREASED ( 21 FDA reports)
DIARRHOEA ( 21 FDA reports)
PAIN IN EXTREMITY ( 21 FDA reports)
DEPRESSION ( 20 FDA reports)
MALAISE ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
CARDIAC DISORDER ( 17 FDA reports)
INJURY ( 17 FDA reports)
OCULAR HYPERAEMIA ( 17 FDA reports)
COUGH ( 16 FDA reports)
ANAEMIA ( 15 FDA reports)
CONTUSION ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
DEHYDRATION ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
MULTIPLE INJURIES ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
BACK PAIN ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
DIABETES MELLITUS ( 13 FDA reports)
DRY EYE ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
SYNCOPE ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
BLOOD GLUCOSE DECREASED ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
TENOSYNOVITIS ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
BREAST CANCER FEMALE ( 10 FDA reports)
BREAST CYST ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
VIRAL INFECTION ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
EYE INJURY ( 9 FDA reports)
HEART RATE IRREGULAR ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
IRITIS ( 9 FDA reports)
LACRIMATION INCREASED ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
PRESYNCOPE ( 9 FDA reports)
PROTEINURIA ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
CORNEAL ABRASION ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
BLINDNESS ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
EYE DISORDER ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FASCIAL INFECTION ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
OSTEITIS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ANHEDONIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
CORNEAL THINNING ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RALES ( 6 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CORNEAL OEDEMA ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
RASH ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ULCER ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ACHLORHYDRIA ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COLON ADENOMA ( 4 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENDOPHTHALMITIS ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FAMILY STRESS ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
IRIDOCELE ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RETINAL CYST ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SLEEP-RELATED EATING DISORDER ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GENITAL PAIN ( 3 FDA reports)
GOITRE ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
VITRITIS ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTERIOR CHAMBER CELL ( 2 FDA reports)
ANTERIOR CHAMBER FLARE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CRANIAL NERVE INJURY ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYCLITIC MEMBRANE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GARDNERELLA INFECTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOTONY OF EYE ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
IRIS BOMBE ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MACULAR ISCHAEMIA ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNION ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CILIARY HYPERAEMIA ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID SENSORY DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE NERVE INJURY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARYNGITIS VIRAL ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use