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

FLUSHING ( 5 FDA reports)
PARAESTHESIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
STRESS ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
FEAR ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CATARACT ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)

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