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

HYPERGLYCAEMIA ( 99 FDA reports)
HYPOGLYCAEMIA ( 71 FDA reports)
BLOOD GLUCOSE INCREASED ( 30 FDA reports)
INJECTION SITE PAIN ( 22 FDA reports)
VOMITING ( 19 FDA reports)
DIABETIC KETOACIDOSIS ( 18 FDA reports)
DIZZINESS ( 18 FDA reports)
FATIGUE ( 18 FDA reports)
PRODUCT QUALITY ISSUE ( 18 FDA reports)
CATARACT ( 17 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
WEIGHT DECREASED ( 17 FDA reports)
WEIGHT INCREASED ( 17 FDA reports)
EYE HAEMORRHAGE ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
FALL ( 13 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
VISUAL IMPAIRMENT ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
BLINDNESS ( 8 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 8 FDA reports)
INJECTION SITE HAEMORRHAGE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
TREMOR ( 8 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PAIN ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
CORONARY ARTERY BYPASS ( 6 FDA reports)
DIABETIC RETINOPATHY ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
COUGH ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HUNGER ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
KETOSIS ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BENIGN MUSCLE NEOPLASM ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THIRST ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NODULE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER NEUROLOGIC ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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