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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127169102 | 12716910 | 2 | F | 20160707 | 20160905 | 20160906 | 20160906 | EXP | FR-PFIZER INC-2016410265 | PFIZER | 70.00 | YR | M | Y | 0.00000 | 20160906 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127169102 | 12716910 | 1 | PS | RAPAMUNE | SIROLIMUS | 1 | Oral | 2 MG, 1X/DAY | Y | 21110 | 2 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127169102 | 12716910 | 1 | Polyarteritis nodosa |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127169102 | 12716910 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127169102 | 12716910 | Immunosuppressant drug level increased | |
| 127169102 | 12716910 | Overdose | |
| 127169102 | 12716910 | Product use issue | |
| 127169102 | 12716910 | Thrombocytopenia |
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 |
|---|---|---|---|---|---|---|
| 127169102 | 12716910 | 1 | 20160623 | 0 |