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

DRUG INEFFECTIVE ( 65 FDA reports)
MYOCARDIAL INFARCTION ( 52 FDA reports)
CONDITION AGGRAVATED ( 51 FDA reports)
HYPERTENSION ( 42 FDA reports)
DIZZINESS ( 35 FDA reports)
CEREBROVASCULAR ACCIDENT ( 34 FDA reports)
PAIN ( 34 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 31 FDA reports)
BLOOD PRESSURE INCREASED ( 31 FDA reports)
DRUG EFFECT DECREASED ( 31 FDA reports)
FEELING ABNORMAL ( 28 FDA reports)
FATIGUE ( 26 FDA reports)
LOSS OF CONSCIOUSNESS ( 26 FDA reports)
ARTHRITIS ( 25 FDA reports)
PAIN IN EXTREMITY ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
TREATMENT NONCOMPLIANCE ( 21 FDA reports)
DIFFICULTY IN WALKING ( 20 FDA reports)
FALL ( 20 FDA reports)
HYPOAESTHESIA ( 19 FDA reports)
MALAISE ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
VISION BLURRED ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
DYSPNOEA ( 18 FDA reports)
FLUSHING ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
VOMITING ( 18 FDA reports)
BACK PAIN ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
ARTHRALGIA ( 16 FDA reports)
CORONARY ARTERY OCCLUSION ( 16 FDA reports)
TREMOR ( 16 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
SOMNOLENCE ( 15 FDA reports)
ABASIA ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
CARDIAC DISORDER ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
HEART RATE IRREGULAR ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 12 FDA reports)
BODY HEIGHT DECREASED ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
COUGH ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
PROSTATE CANCER ( 9 FDA reports)
AMNESIA ( 8 FDA reports)
BLOOD PRESSURE ABNORMAL ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
MEDICATION ERROR ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
VISUAL DISTURBANCE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PROCEDURAL PAIN ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
COMA ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
OCULAR VASCULAR DISORDER ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FEAR ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
SCAR ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
STRESS ( 5 FDA reports)
SWELLING ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLINDNESS TRANSIENT ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EYE REDNESS ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SURGERY ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SNORING ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TETANY ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIGRATION OF IMPLANT ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE OPERATION ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INFUSION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION CRYSTALS IN URINE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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