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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123864953 | 12386495 | 3 | F | 20151201 | 20160822 | 20160519 | 20160829 | PER | US-CELGENEUS-USA-2016047450 | CELGENE | 67.05 | YR | M | Y | 0.00000 | 20160829 | PH | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123864953 | 12386495 | 1 | PS | THALOMID | THALIDOMIDE | 1 | Oral | U | B80028AH | 20785 | 50 | MG | CAPSULES | QD | |||||
123864953 | 12386495 | 2 | SS | THALOMID | THALIDOMIDE | 1 | Oral | U | B80028AH | 20785 | 50 | MG | CAPSULES | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123864953 | 12386495 | 1 | Plasma cell myeloma |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123864953 | 12386495 | Acne | |
123864953 | 12386495 | Dizziness | |
123864953 | 12386495 | Fatigue | |
123864953 | 12386495 | Somnolence | |
123864953 | 12386495 | Tooth abscess |
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 |
---|---|---|---|---|---|---|
123864953 | 12386495 | 1 | 20150622 | 0 | ||
123864953 | 12386495 | 2 | 20150723 | 0 |