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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8623746 | 8533203 | F | 8623746-8 | 20081223 | 20120821 | 20120827 | EXP | US-PFIZER INC-2012102151 | PFIZERINC | YR | F | Y | 2.9 | KG | 20120827 | LW | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8623746 | 1020671051 | C | CHANTIX | 1 | TRANSPLACENTAL | STARTER PACK | |||||
8623746 | 1020671050 | PS | EFFEXOR | 1 | TRANSPLACENTAL | 75 MG, 1X/DAY | 020151 | ||||
8623746 | 1020671053 | C | ZOFRAN | 1 | TRANSPLACENTAL | 8 MG, 1X/DAY | |||||
8623746 | 1020671052 | C | CHANTIX | 1 | TRANSPLACENTAL | 1 MG, 2X/DAY |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8623746 | 1020671050 | MAJOR DEPRESSION |
Outcome of event
Event ID | OUTC COD |
---|---|
8623746 | CA |
8623746 | OT |
Reactions reported
Event ID | PT |
---|---|
8623746 | MATERNAL EXPOSURE DURING PREGNANCY |
8623746 | DEVELOPMENTAL DELAY |
8623746 | CONGENITAL ANOMALY |
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 |
---|---|---|---|---|---|
8623746 | 1020671051 | 20081024 | |||
8623746 | 1020671050 | 20080804 | 20081223 | 142 | DAY |
8623746 | 1020671053 | 20080630 | 20 | DAY | |
8623746 | 1020671052 | 20081107 |