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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016618 | 8317509 | I | 8016618-3 | 20111223 | 20111231 | EXP | CHPA2011US018588 | NOVARTIS CONSUMER HEALTH, INC. | 77 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016618 | 1018419888 | PS | EXCEDRIN TENSION HEADACHE | 2 | ORAL | 8 CAPLETS PER DAY | 10122521 | ||||
| 8016618 | 1018419889 | SS | EXCEDRIN TENSION HEADACHE | 2 | ORAL | 2 CAPLETS PER DAY | 10122521 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016618 | 1018419888 | BACK PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016618 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8016618 | SCIATICA |
| 8016618 | FALL |
| 8016618 | INCORRECT DRUG ADMINISTRATION DURATION |
| 8016618 | BACK PAIN |
| 8016618 | INTERVERTEBRAL DISC PROTRUSION |
| 8016618 | OFF LABEL USE |
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 |
|---|---|---|---|---|---|
| 8016618 | 1018419888 | 19900101 | 20060101 | ||
| 8016618 | 1018419889 | 20060101 |