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
125490241 12549024 1 I 20160608 20160630 20160712 20160712 EXP FR-PFIZER INC-2016326223 PFIZER 69.00 YR M Y 0.00000 20160712 OT FR FR

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
125490241 12549024 1 PS Carboplatine Hospira CARBOPLATIN 1 Intravenous drip UNK 77059 SOLUTION FOR INJECTION
125490241 12549024 2 SS ALIMTA PEMETREXED DISODIUM 1 Intravenous drip UNK 0 POWDER FOR SOLUTION FOR INFUSION
125490241 12549024 3 C ATORVASTATIN ATORVASTATIN 1 UNK 0
125490241 12549024 4 C XGEVA DENOSUMAB 1 UNK 0
125490241 12549024 5 C ASPIRINE ASPIRIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125490241 12549024 1 Lung adenocarcinoma stage IV
125490241 12549024 2 Lung adenocarcinoma stage IV

Outcome of event

Event ID CASEID OUTC COD
125490241 12549024 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125490241 12549024 Hepatocellular injury

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
125490241 12549024 1 20160601 0
125490241 12549024 2 20160601 20160601 0
125490241 12549024 3 201606 0
125490241 12549024 4 20160523 0
125490241 12549024 5 201606 0