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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016607 | 8317498 | I | 8016607-9 | 20100101 | 20111222 | 20111231 | EXP | CHPA2011US018564 | NOVARTIS CONSUMER HEALTH, INC. | 56 | YR | M | Y | 20111230 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016607 | 1018419866 | SS | EXCEDRIN (MIGRAINE) | 1 | ORAL | UNK, UNK | 10115590 | ||||
| 8016607 | 1018419867 | SS | EXCEDRIN TENSION HEADACHE | 2 | ORAL | UNK, UNK | 10115690 | ||||
| 8016607 | 1018419865 | PS | EXCEDRIN (MIGRAINE) | 1 | ORAL | 2 DF, UNK | 10116783 | 020802 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016607 | 1018419866 | MIGRAINE |
| 8016607 | 1018419867 | MIGRAINE |
| 8016607 | 1018419865 | MIGRAINE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016607 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8016607 | HYPERTENSION |
| 8016607 | MIGRAINE |
| 8016607 | THERAPEUTIC RESPONSE DECREASED |
| 8016607 | DEPRESSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |