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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125608901 | 12560890 | 1 | I | 20150911 | 20150916 | 20160715 | 20160715 | EXP | IT-MINISAL02-325585 | IT-PFIZER INC-3012824 | PFIZER | 66.00 | YR | F | Y | 68.00000 | KG | 20160715 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125608901 | 12560890 | 1 | PS | CEFAZOLIN | CEFAZOLIN | 1 | Intramuscular | 2 G, TOTAL | 65226 | 2 | G | POWDER FOR SOLUTION FOR INJECTION | |||||||
| 125608901 | 12560890 | 2 | SS | VANCOMYCIN HCL | VANCOMYCIN HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 1 G, TOTAL | 62911 | 1 | G |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125608901 | 12560890 | 1 | Antibiotic prophylaxis |
| 125608901 | 12560890 | 2 | Antibiotic prophylaxis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125608901 | 12560890 | Erythema | |
| 125608901 | 12560890 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 125608901 | 12560890 | 2 | 20150911 | 20150911 | 0 |