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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126639391 | 12663939 | 1 | I | 20160527 | 20160810 | 20160818 | 20160818 | EXP | CN-PFIZER INC-2016385136 | PFIZER | 66.00 | YR | F | Y | 52.00000 | KG | 20160818 | OT | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126639391 | 12663939 | 1 | PS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous drip | 40 MG, 2X/DAY | Y | L191060 | 11856 | 40 | MG | POWDER FOR SOLUTION FOR INJECTION | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126639391 | 12663939 | 1 | Infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126639391 | 12663939 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126639391 | 12663939 | Asthma | |
| 126639391 | 12663939 | Chest discomfort | |
| 126639391 | 12663939 | Disease recurrence | |
| 126639391 | 12663939 | Dyspnoea | |
| 126639391 | 12663939 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 126639391 | 12663939 | 1 | 20160527 | 20160527 | 0 |