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
100811103 10081110 3 F 20131209 20140917 20140416 20140930 EXP IT-MYLANLABS-2014S1007857 MYLAN 0.00 Y 0.00000 20140930 N MD IT IT

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
100811103 10081110 1 PS PACLITAXEL. PACLITAXEL 1 INTRAVENOUS 175 MG,CYCLE D 75278 175 MG POWDER FOR SOLUTION FOR INFUSION
100811103 10081110 2 SS CARBOPLATINO TEVA CARBOPLATIN 1 INTRAVENOUS 250 MG,CYCLE D 0 250 MG POWDER FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100811103 10081110 1 Ovarian cancer stage I
100811103 10081110 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100811103 10081110 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100811103 10081110 Asthenia
100811103 10081110 Electrolyte imbalance
100811103 10081110 Nausea
100811103 10081110 Neutropenia
100811103 10081110 Stomatitis
100811103 10081110 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
100811103 10081110 1 20131202 20131202 0
100811103 10081110 2 20131202 0