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

HYPOGLYCAEMIA ( 54 FDA reports)
HYPERGLYCAEMIA ( 28 FDA reports)
BLOOD GLUCOSE INCREASED ( 26 FDA reports)
MYOCARDIAL INFARCTION ( 26 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 24 FDA reports)
DEATH ( 20 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 19 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
PRODUCT QUALITY ISSUE ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 13 FDA reports)
KETOACIDOSIS ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
HOSPITALISATION ( 9 FDA reports)
VOMITING ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
GASTROINTESTINAL CARCINOMA ( 7 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
CATARACT ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
COUGH ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FALL ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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