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

URGE INCONTINENCE ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FALL ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)

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