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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126164712 | 12616471 | 2 | F | 20160802 | 20160802 | 20160803 | EXP | US-PFIZER INC-2016148040 | PFIZER | 0.00 | M | Y | 0.00000 | 20160803 | PH | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126164712 | 12616471 | 1 | SS | AMPHOTERICIN B LIPID COMPLEX | AMPHOTERICIN B | 1 | UNK | U | 0 | ||||||||||
| 126164712 | 12616471 | 2 | PS | HYDROCORTISONE. | HYDROCORTISONE | 1 | UNK | U | 8697 | TABLET | |||||||||
| 126164712 | 12616471 | 3 | SS | MEROPENEM. | MEROPENEM | 1 | UNK | U | 90940 | ||||||||||
| 126164712 | 12616471 | 4 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | UNK | U | 20987 | ||||||||||
| 126164712 | 12616471 | 5 | SS | VANCOMYCIN HCL | VANCOMYCIN HYDROCHLORIDE | 1 | UNK | U | 62911 | ||||||||||
| 126164712 | 12616471 | 6 | SS | ACYCLOVIR. | ACYCLOVIR | 1 | UNK | U | 0 | ||||||||||
| 126164712 | 12616471 | 7 | SS | CASPOFUNGIN | CASPOFUNGIN | 1 | UNK | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126164712 | 12616471 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126164712 | 12616471 | Neutropenia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |