The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126220221 12622022 1 I 20160629 20160722 20160804 20160804 EXP IT-PFIZER INC-2016360182 PFIZER 74.00 YR M Y 0.00000 20160804 MD IT IT

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126220221 12622022 1 PS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1804 MG, CYCLIC Y 78339 1804 MG
126220221 12622022 2 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) 468 MG, CYCLIC Y 76517 468 MG
126220221 12622022 3 C DEXAMETHASONE PHOSPHATE DEXAMETHASONE PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126220221 12622022 1 Bladder cancer
126220221 12622022 2 Bladder cancer

Outcome of event

Event ID CASEID OUTC COD
126220221 12622022 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126220221 12622022 Anaemia
126220221 12622022 Rash erythematous
126220221 12622022 Septic embolus
126220221 12622022 Staphylococcal sepsis
126220221 12622022 Thrombocytopenia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126220221 12622022 1 20160518 20160616 0
126220221 12622022 2 20160518 20160616 0