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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
102460371 | 10246037 | 1 | I | 201301 | 20130206 | 20130215 | 20130215 | EXP | 2013-0685 | IPSEN | 54.00 | YR | F | N | 0.00000 | 20130214 | N | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
102460371 | 10246037 | 1 | PS | SOMATULINE DEPOT INJECTION | 1 | D | D | 22074 | 120 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
102460371 | 10246037 | 1 | Acromegaly |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
102460371 | 10246037 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
102460371 | 10246037 | Chest pain | |
102460371 | 10246037 | Pulmonary mass | |
102460371 | 10246037 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
102460371 | 10246037 | CSM |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
102460371 | 10246037 | 1 | 201004 | 0 |