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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387738 | 7143989 | F | 1 | 6387738-4 | 20090901 | 20090922 | 20090930 | EXP | 1-19884376 | MEDICIS PHARMACEUTICAL CORPORATION | 13 | YR | F | N | 120 | LBS | 20090929 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387738 | 1012374797 | PS | SOLODYN | 1 | ORAL | 90 MG ONCE DAILY, ORAL | N | D | 50808 | ||
| 6387738 | 1012432676 | C | ZYRTEC | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6387738 | 1012374797 | ACNE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6387738 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6387738 | BENIGN INTRACRANIAL HYPERTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6387738 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6387738 | 1012374797 | 20090624 | 20090906 |