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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107511114 | 10751111 | 4 | F | 20160624 | 20150130 | 20160722 | PER | US-PFIZER INC-2015034666 | PFIZER | 49.00 | YR | M | Y | 0.00000 | 20160722 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107511114 | 10751111 | 1 | PS | RAPAMUNE | SIROLIMUS | 1 | Oral | 0.5 MG, UNK | 21083 | .5 | MG | ORAL SOLUTION | |||||||
| 107511114 | 10751111 | 2 | C | VFEND | VORICONAZOLE | 1 | 200 MG, UNK | 0 | 200 | MG | |||||||||
| 107511114 | 10751111 | 3 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107511114 | 10751111 | 1 | Bone marrow transplant |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107511114 | 10751111 | Product use issue | |
| 107511114 | 10751111 | Pruritus | |
| 107511114 | 10751111 | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |