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BLOOD GLUCOSE INCREASED ( 7 FDA reports)
NAUSEA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POLYP ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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