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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4543974 | 5710032 | I | 4543974-0 | 20040908 | 20040909 | 20040103 | PER | US-JNJFOC-20040903840 | JOHNSON + JOHNSON PHARMACEUTICAL | 27 | YR | F | N | 115 | LBS | 20041208 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4543974 | 1005552277 | PS | ORTHO EVRA | 1 | TRANSDERMAL | 1 DOSE(S), 3 IN 4 WEEK, TRANSDERMAL | D | D | 21180 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4543974 | 1005552277 | CONTRACEPTION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4543974 | DIZZINESS |
| 4543974 | FATIGUE |
| 4543974 | WITHDRAWAL BLEED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4543974 | CSM |
Therapies reported
| no results found |