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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8553555 | 8694490 | I | 8553555-X | 20120726 | 20120731 | PER | US-PFIZER INC-2012181749 | PFIZERINC | YR | F | Y | 20120731 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8553555 | 1020401944 | PS | IBUPROFEN | 1 | UNK | 18989 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
8553555 | DRUG HYPERSENSITIVITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |