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
125115602 12511560 2 F 201501 20160817 20160629 20160825 EXP NO-NOMAADVRE-NOMAADVRE-2016-22131 NO-009507513-1605NOR009303 MERCK 69.00 YR M Y 0.00000 20160825 OT NO NO

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
125115602 12511560 1 PS TEMOZOLOMIDE. TEMOZOLOMIDE 1 Oral 160 MG DAILY, BASED ON A BODY SURFACE AREA OF 2.1 M2 U 21029 160 MG CAPSULE QD
125115602 12511560 2 SS TEMOZOLOMIDE. TEMOZOLOMIDE 1 U 21029 CAPSULE
125115602 12511560 3 C ENALAPRIL MALEATE. ENALAPRIL MALEATE 1 Oral UNK U 0 TABLET
125115602 12511560 4 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral UNK U 0 TABLET
125115602 12511560 5 C LANZOPRAZOL LANSOPRAZOLE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125115602 12511560 1 Glioblastoma multiforme
125115602 12511560 2 Chemotherapy
125115602 12511560 4 Hypertension
125115602 12511560 5 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
125115602 12511560 OT
125115602 12511560 HO
125115602 12511560 DE
125115602 12511560 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125115602 12511560 Bone marrow failure
125115602 12511560 Death
125115602 12511560 Decreased appetite
125115602 12511560 Lethargy
125115602 12511560 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
125115602 12511560 1 20150105 20150128 0