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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5903476 | 6775421 | I | 5903476-3 | 20080922 | 20080930 | PER | US-BAYER-200813859BCC | BAYER HEALTHCARE LLC | M | Y | 20080930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5903476 | 1010520647 | PS | ALEVE | 1 | UNK | 020204 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5903476 | 1010520647 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
5903476 | HO |
Reactions reported
Event ID | PT |
---|---|
5903476 | HYPERSENSITIVITY |
5903476 | SKIN DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |