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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8016606 | 8286190 | F | 8016606-7 | 20111230 | 20111231 | EXP | GB-ACCORD-011469 | ACCORDHCP | 35 | YR | F | Y | 20111231 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8016606 | 1018419863 | PS | FINASTERIDE | 1 | 090121 | ||||||
8016606 | 1018419864 | C | FOLIC ACID | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8016606 | 1018419863 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8016606 | OT |
Reactions reported
Event ID | PT |
---|---|
8016606 | MATERNAL EXPOSURE DURING PREGNANCY |
8016606 | ACCIDENTAL EXPOSURE |
8016606 | NO ADVERSE EVENT |
8016606 | WRONG TECHNIQUE IN DRUG USAGE PROCESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |