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BLOOD GLUCOSE INCREASED ( 12 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
VOMITING ( 3 FDA reports)
TREMOR ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
COUGH ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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