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

BLOOD PRESSURE INCREASED ( 34 FDA reports)
HYPERTENSION ( 28 FDA reports)
DRUG INEFFECTIVE ( 22 FDA reports)
SOMNOLENCE ( 13 FDA reports)
DIZZINESS ( 12 FDA reports)
HEADACHE ( 11 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
ANAEMIA ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
VOMITING ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AGITATION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
FALL ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SWELLING ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
COMA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOPOR ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use