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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96087061 | 9608706 | 1 | I | 20130928 | 0 | 20131007 | 20131007 | DIR | 44.00 | YR | A | F | N | 76.20000 | KG | 20131004 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96087061 | 9608706 | 1 | PS | NULOJIX | BELATACEPT | 1 | INTRAVENOUS | 400 MG, QM, IV | D | D | 3A77180 | 20150930 | 0 | 400 | MG | QM | |||
| 96087061 | 9608706 | 2 | SS | CELLCEPT | MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE | 1 | ORAL | 1 G, BID, PO | D | D | 0 | 1 | GM | BID | |||||
| 96087061 | 9608706 | 4 | C | ALEMTUZUMAB | ALEMTUZUMAB | 1 | 0 | ||||||||||||
| 96087061 | 9608706 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 96087061 | 9608706 | 1 | Renal transplant |
| 96087061 | 9608706 | 2 | Renal transplant |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 96087061 | 9608706 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 96087061 | 9608706 | Abdominal pain lower | |
| 96087061 | 9608706 | Nausea | |
| 96087061 | 9608706 | Transplant rejection | |
| 96087061 | 9608706 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 96087061 | 9608706 | HP |
Therapies reported
| no results found |