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
126385501 12638550 1 I 20160729 20160809 20160809 EXP GB-SA-2016SA139490 AVENTIS 0.00 A F Y 0.00000 20160809 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
126385501 12638550 1 PS DOCETAXEL. DOCETAXEL 1 Unknown U UNKNOWN 20449
126385501 12638550 2 SS CARBOPLATIN. CARBOPLATIN 1 Unknown U UNKNOWN 0
126385501 12638550 3 SS HERCEPTIN TRASTUZUMAB 1 Unknown U UNKNOWN 0
126385501 12638550 4 SS PERJETA PERTUZUMAB 1 Unknown U UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126385501 12638550 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126385501 12638550 Haematotoxicity
126385501 12638550 Neuropathy peripheral

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

no results found

Therapies reported

no results found