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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5119566 | 6145290 | I | 5119566-1 | 20060919 | 20060929 | EXP | 2006112599 | PFIZER INC. | 25 | YR | F | N | 153 | LBS | 20060928 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5119566 | 1007725044 | PS | SERTRALINE | 1 | 100 MG (100 MG, 1 IN 1 D) | U | U | 19839 | |||
5119566 | 1007749361 | C | TRICYCLEN (ETHINYLESTRADIOL, NORGESTIMATE) | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5119566 | 1007725044 | OBSESSIVE-COMPULSIVE DISORDER |
Outcome of event
Event ID | OUTC COD |
---|---|
5119566 | DS |
5119566 | OT |
Reactions reported
Event ID | PT |
---|---|
5119566 | DIZZINESS |
5119566 | DYSSTASIA |
5119566 | HEADACHE |
5119566 | NAUSEA |
5119566 | PUPILS UNEQUAL |
5119566 | THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION |
5119566 | VISION BLURRED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5119566 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5119566 | 1007725044 | 1 | WK |