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
127138441 12713844 1 I 20160901 20160905 20160905 EXP DE-009507513-1609DEU000588 MERCK 67.00 YR F Y 0.00000 20160905 MD DE DE

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
127138441 12713844 1 PS TEMODAL TEMOZOLOMIDE 1 Oral U 21029 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127138441 12713844 1 Astrocytoma

Outcome of event

Event ID CASEID OUTC COD
127138441 12713844 DS
127138441 12713844 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127138441 12713844 Fall
127138441 12713844 Gait disturbance
127138441 12713844 Helplessness
127138441 12713844 Neuropathy peripheral
127138441 12713844 Prescribed overdose
127138441 12713844 Product use issue
127138441 12713844 Walking aid user

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

no results found

Therapies reported

no results found