Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8555117 | 8695683 | I | 8555117-7 | 20120724 | 20120725 | 20120731 | EXP | US-PFIZER INC-2012181556 | PFIZERINC | 1 | YR | M | Y | 20120731 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8555117 | 1020408343 | PS | EPIPEN JR. | 1 | UNK | 019430 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8555117 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8555117 | INJECTION SITE INJURY |
| 8555117 | INJECTION SITE HAEMATOMA |
| 8555117 | PRODUCT QUALITY ISSUE |
| 8555117 | INJECTION SITE PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8555117 | 1020408343 | 20120724 |