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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127322631 | 12732263 | 1 | I | 20160830 | 20160902 | 20160912 | 20160912 | EXP | PHHO2016NL013030 | NOVARTIS | 63.66 | YR | M | Y | 95.00000 | KG | 20160912 | MD | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127322631 | 12732263 | 1 | PS | CERTICAN | EVEROLIMUS | 1 | Oral | 3 MG, BID | 2052 | MG | U | 21560 | 3 | MG | TABLET | BID | |||
| 127322631 | 12732263 | 2 | SS | PROGRAF | TACROLIMUSTACROLIMUS ANHYDROUS | 1 | Unknown | 2 MG, BID | 1372 | MG | U | U | 0 | 2 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127322631 | 12732263 | 1 | Renal transplant |
| 127322631 | 12732263 | 2 | Renal transplant |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127322631 | 12732263 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127322631 | 12732263 | Pyrexia | |
| 127322631 | 12732263 | Respiratory failure |
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 |
|---|---|---|---|---|---|---|
| 127322631 | 12732263 | 1 | 20150923 | 20160829 | 0 | |
| 127322631 | 12732263 | 2 | 20150922 | 20160829 | 0 |