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
126242471 12624247 1 I 201512 20160725 20160805 20160805 EXP US-ROCHE-1802185 ROCHE 45.34 YR F Y 65.50000 KG 20160805 MD US US

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
126242471 12624247 1 PS AVASTIN BEVACIZUMAB 1 Unknown Y 125085
126242471 12624247 2 SS CISPLATIN. CISPLATIN 1 Unknown 0
126242471 12624247 3 SS TAXOL PACLITAXEL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126242471 12624247 1 Cervix carcinoma
126242471 12624247 2 Cervix carcinoma
126242471 12624247 3 Cervix carcinoma

Outcome of event

Event ID CASEID OUTC COD
126242471 12624247 OT
126242471 12624247 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126242471 12624247 Abdominal pain
126242471 12624247 Gastroenteritis radiation
126242471 12624247 Haematochezia
126242471 12624247 Large intestine perforation
126242471 12624247 Nausea
126242471 12624247 Vomiting

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
126242471 12624247 1 201508 201512 0
126242471 12624247 2 201508 0
126242471 12624247 3 201508 0