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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6523389 | 7234929 | I | 6523389-6 | 20091229 | 20091231 | PER | BR-ROCHE-676833 | ROCHE | F | Y | 65 | KG | 20091231 | CN | BRAZIL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6523389 | 1012885609 | PS | ROACUTAN | 2 | ORAL | 18662 | |||||
6523389 | 1012885610 | C | CONTRACEPTIVE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6523389 | 1012885609 | ACNE |
6523389 | 1012885610 | CONTRACEPTION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6523389 | NO ADVERSE EVENT |
6523389 | PREGNANCY |
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 |
---|---|---|---|---|---|
6523389 | 1012885609 | 20090701 | 20091115 | ||
6523389 | 1012885610 | 20090101 |