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
127746431 12774643 1 I 20160805 20160915 20160923 20160923 EXP FR-009507513-1609FRA008486 MERCK 78.35 YR M Y 62.00000 KG 20160923 OT FR FR

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
127746431 12774643 1 PS TEMODAL TEMOZOLOMIDE 1 Oral 260 MG, QD 1300 MG D 21029 260 MG CAPSULE QD
127746431 12774643 2 C PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 UNK 0
127746431 12774643 3 C ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 Oral UNK 0 CAPSULE
127746431 12774643 4 C SOLUPRED PREDNISOLONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127746431 12774643 1 Glioblastoma

Outcome of event

Event ID CASEID OUTC COD
127746431 12774643 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127746431 12774643 Anaemia
127746431 12774643 Asthenia
127746431 12774643 Decreased appetite
127746431 12774643 Weight decreased

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
127746431 12774643 1 20160730 20160803 0