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

ABDOMINAL PAIN ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PORPHYRIA ACUTE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHOLECYSTOSTOMY ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTESTINAL T-CELL LYMPHOMA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
RASH ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)

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