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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127821221 | 12782122 | 1 | I | 20160817 | 0 | 20160923 | 20160923 | DIR | FDA-CTU | 73.00 | YR | F | N | 140.00000 | LBS | 20160818 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127821221 | 12782122 | 1 | PS | LENALIDOMIDE | LENALIDOMIDE | 1 | Oral | LENALIDOMIDE 15 MG, DAYS 1-21, PO | 0 | 15 | MG | ||||||||
127821221 | 12782122 | 2 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Oral | DEXAMETHASONE 8MG, DAYS 1, 8, 15, 22 - PO | 0 | 8 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127821221 | 12782122 | 1 | Plasma cell myeloma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127821221 | 12782122 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127821221 | 12782122 | Colitis | |
127821221 | 12782122 | Diarrhoea | |
127821221 | 12782122 | Nausea | |
127821221 | 12782122 | Rectal haemorrhage | |
127821221 | 12782122 | Vomiting |
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 |
---|---|---|---|---|---|---|
127821221 | 12782122 | 1 | 20160201 | 20160815 | 0 | |
127821221 | 12782122 | 2 | 20160201 | 20160809 | 0 |