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

TREMOR ( 5 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
SOMNOLENCE ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAIN ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
COUGH ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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