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
126764622 12676462 2 F 20160822 20160823 20160902 EXP GB-TEVA-684558ACC TEVA 0.00 F Y 0.00000 20160902 CN GB GB

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
126764622 12676462 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown TWO CYCLES N 77269
126764622 12676462 2 SS PEMETREXED PEMETREXED 1 THREE CYCLES U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126764622 12676462 1 Non-small cell lung cancer
126764622 12676462 2 Non-small cell lung cancer

Outcome of event

Event ID CASEID OUTC COD
126764622 12676462 OT
126764622 12676462 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126764622 12676462 Asthenia
126764622 12676462 Diarrhoea
126764622 12676462 Full blood count decreased

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

no results found

Therapies reported

no results found