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

DIZZINESS ( 31 FDA reports)
FALL ( 29 FDA reports)
ASTHENIA ( 28 FDA reports)
VOMITING ( 28 FDA reports)
HYPERTENSION ( 27 FDA reports)
PNEUMONIA ( 26 FDA reports)
SOMNOLENCE ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
NAUSEA ( 24 FDA reports)
PAIN ( 24 FDA reports)
BLOOD PRESSURE INCREASED ( 23 FDA reports)
SYNCOPE ( 23 FDA reports)
DYSPNOEA ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
HYPERGLYCAEMIA ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
CHEST PAIN ( 19 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
MEMORY IMPAIRMENT ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
MALAISE ( 18 FDA reports)
DEPRESSION ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
HYPOGLYCAEMIA ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
INFARCTION ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
CONSTIPATION ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
ANGIOPLASTY ( 14 FDA reports)
COMA ( 14 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
COUGH ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
DEATH ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
INFLUENZA ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
EPILEPSY ( 10 FDA reports)
INTESTINAL OBSTRUCTION ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
AGITATION ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
BONE PAIN ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
ISCHAEMIA ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
SWELLING ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
VENOUS OCCLUSION ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CORONARY ARTERY BYPASS ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MASS ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SURGERY ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
WOUND ( 5 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ARTERIAL REPAIR ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHOKING ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SPIDER NAEVUS ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYST ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GASTROINTESTINAL SURGERY ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NODULE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCARDITIS RHEUMATIC ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JUVENILE MELANOMA BENIGN ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN OPERATION ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)

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