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

SOMNOLENCE ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
COUGH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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