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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127203192 | 12720319 | 2 | F | 20160816 | 20160826 | 20160907 | 20160908 | EXP | DE-BFARM-16290186 | DE-GLAXOSMITHKLINE-DE2016GSK128368 | GLAXOSMITHKLINE | 76.00 | YR | M | Y | 92.00000 | KG | 20160908 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127203192 | 12720319 | 1 | PS | CEFUROXIME. | CEFUROXIME | 1 | Intravenous (not otherwise specified) | 1500 MG, UNK | U | 50605 | 1500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127203192 | 12720319 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127203192 | 12720319 | LT |
| 127203192 | 12720319 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127203192 | 12720319 | Anaphylactic shock | |
| 127203192 | 12720319 | Cardiac arrest | |
| 127203192 | 12720319 | Resuscitation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |