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

DEVICE MALFUNCTION ( 107 FDA reports)
WRONG DRUG ADMINISTERED ( 72 FDA reports)
PRODUCT QUALITY ISSUE ( 53 FDA reports)
HYPOGLYCAEMIA ( 45 FDA reports)
HYPERGLYCAEMIA ( 30 FDA reports)
ASTHENIA ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
COLD SWEAT ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
VOMITING ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
KETOACIDOSIS ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PAIN ( 5 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
KETONURIA ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)

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