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
126475201 12647520 1 I 20160715 0 20160811 20160811 DIR 47.62 YR F N 127.50000 KG 20160801 N MD 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
126475201 12647520 1 PS TAXOL PACLITAXEL 1 0 175 MG
126475201 12647520 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0
126475201 12647520 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126475201 12647520 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126475201 12647520 Bronchitis
126475201 12647520 Chills
126475201 12647520 Fatigue
126475201 12647520 Headache
126475201 12647520 Mucosal inflammation
126475201 12647520 Nausea
126475201 12647520 Neck pain
126475201 12647520 Palmar-plantar erythrodysaesthesia syndrome
126475201 12647520 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
126475201 12647520 1 20160705 0
126475201 12647520 2 20160510 0
126475201 12647520 3 20160510 0