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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125106903 | 12510690 | 3 | F | 201501 | 20160819 | 20160629 | 20160831 | EXP | NO-NOMAADVRE-NOMAADVRE-2016-22131 | NO-TEVA-670110ACC | TEVA | VANDRAAS K,TJONNFJORD G,JOHANNESEN T,BRANDAL P. | 69.00 | YR | M | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125106903 | 12510690 | 1 | PS | TEMOZOLOMIDE. | TEMOZOLOMIDE | 1 | Oral | 160 MILLIGRAM DAILY; TMZ DOSE OF 160 MG DAILY, BASED ON A BODY SURFACE AREA OF 2.1 M2 | 78879 | 160 | MG | CAPSULE | QD | ||||||
| 125106903 | 12510690 | 2 | SS | TEMOZOLOMIDE. | TEMOZOLOMIDE | 1 | 78879 | CAPSULE | |||||||||||
| 125106903 | 12510690 | 3 | C | Enalapril | ENALAPRIL | 1 | Oral | UNK | 0 | TABLET | |||||||||
| 125106903 | 12510690 | 4 | C | LANZOPRAZOL | LANSOPRAZOLE | 1 | UNK | 0 | |||||||||||
| 125106903 | 12510690 | 5 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | UNK | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125106903 | 12510690 | 1 | Glioblastoma multiforme |
| 125106903 | 12510690 | 2 | Chemotherapy |
| 125106903 | 12510690 | 4 | Gastrooesophageal reflux disease |
| 125106903 | 12510690 | 5 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125106903 | 12510690 | OT |
| 125106903 | 12510690 | HO |
| 125106903 | 12510690 | DE |
| 125106903 | 12510690 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125106903 | 12510690 | Bone marrow failure | |
| 125106903 | 12510690 | Death | |
| 125106903 | 12510690 | Decreased appetite | |
| 125106903 | 12510690 | Lethargy | |
| 125106903 | 12510690 | 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 |
|---|---|---|---|---|---|---|
| 125106903 | 12510690 | 1 | 20150105 | 20150128 | 0 |