The Safety Rates Drug Report

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Drug     Injury     Quarter    

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