Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6810137 | 7448874 | I | 6810137-5 | 20070101 | 20100622 | 20100630 | EXP | NL-WATSON-2010-08502 | WATSON | 47 | YR | M | Y | 20100630 | OT | NETHERLANDS |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6810137 | 1014006339 | PS | PREDNISOLONE (WATSON LABORATORIES) | 2 | 10 MG, DAILY | UNCONFIRMED | 80354 | ||||
6810137 | 1014006340 | SS | AZATHIOPRINE | 1 | 175 MG, DAILY |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6810137 | 1014006339 | PROPHYLAXIS AGAINST TRANSPLANT REJECTION |
6810137 | 1014006340 | PROPHYLAXIS AGAINST TRANSPLANT REJECTION |
Outcome of event
Event ID | OUTC COD |
---|---|
6810137 | OT |
Reactions reported
Event ID | PT |
---|---|
6810137 | SQUAMOUS CELL CARCINOMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6810137 | 1014006339 | 9125 | DAY | ||
6810137 | 1014006340 | 9125 | DAY |