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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127174601 | 12717460 | 1 | I | 20160824 | 20160906 | 20160906 | EXP | CN-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123343 | RANBAXY | 54.00 | YR | M | Y | 0.00000 | 20160906 | OT | GB | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127174601 | 12717460 | 1 | SS | MEROPENEM. | MEROPENEM | 1 | Intravenous (not otherwise specified) | Y | U | 0 | 1 | G | Q8H | ||||||
| 127174601 | 12717460 | 2 | PS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | U | U | 84764 | |||||||||
| 127174601 | 12717460 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127174601 | 12717460 | 1 | Product used for unknown indication |
| 127174601 | 12717460 | 2 | Central nervous system lymphoma |
| 127174601 | 12717460 | 3 | Central nervous system lymphoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127174601 | 12717460 | OT |
| 127174601 | 12717460 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127174601 | 12717460 | Drug resistance | |
| 127174601 | 12717460 | Klebsiella infection | |
| 127174601 | 12717460 | Pathogen resistance |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |