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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8016615 | 8317506 | I | 8016615-8 | 20111223 | 20111231 | EXP | CHPA2011US018575 | NOVARTIS CONSUMER HEALTH, INC. | 65 | YR | F | Y | 20111231 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8016615 | 1018419884 | PS | EXCEDRIN (MIGRAINE) | 1 | ORAL | UNK, UNK |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
8016615 | OT |
Reactions reported
Event ID | PT |
---|---|
8016615 | GASTRIC ULCER |
8016615 | INCORRECT DRUG ADMINISTRATION DURATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |