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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5472347 | 6380670 | F | 5472347-1 | 20070920 | 20070930 | EXP | SE-SHR-SE-2006-036743 | BERLEX | F | Y | 56.6 | KG | 20070928 | SWEDEN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5472347 | 1008989635 | PS | YASMIN | 1 | ORAL | 1 TAB(S), 21D/28D | 021098 | ||||
5472347 | 1008989636 | C | ASACOL | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5472347 | OT |
Reactions reported
Event ID | PT |
---|---|
5472347 | HEPATIC STEATOSIS |
5472347 | HEPATITIS |
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 |
---|---|---|---|---|---|
5472347 | 1008989635 | 20050401 |