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
127215701 12721570 1 I 20160617 20160907 20160907 EXP FR-ASTRAZENECA-2016SE68962 ASTRAZENECA 72.00 YR F Y 0.00000 20160907 MD 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
127215701 12721570 1 PS TAGRISSO OSIMERTINIB 1 Oral AZD9291 208065 TABLET
127215701 12721570 2 SS TAGRISSO OSIMERTINIB 1 Oral 208065 80 MG TABLET QD
127215701 12721570 3 SS TAXOL PACLITAXEL 1 Unknown 0
127215701 12721570 4 SS TAXOL PACLITAXEL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127215701 12721570 1 Non-small cell lung cancer
127215701 12721570 2 Non-small cell lung cancer
127215701 12721570 3 Ovarian cancer
127215701 12721570 4 Ovarian cancer

Outcome of event

Event ID CASEID OUTC COD
127215701 12721570 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127215701 12721570 Diarrhoea
127215701 12721570 Onychoclasis
127215701 12721570 Ovarian cancer
127215701 12721570 Paronychia
127215701 12721570 Platelet count decreased

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
127215701 12721570 1 20150520 0