The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126444542 12644454 2 F 2007 20160816 20160811 20160817 PER US-PFIZER INC-2016378709 PFIZER 40.00 YR M Y 0.00000 20160817 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126444542 12644454 1 PS CHANTIX VARENICLINE TARTRATE 1 UNK 21928 FILM-COATED TABLET
126444542 12644454 2 SS CHANTIX VARENICLINE TARTRATE 1 3 MG, 1X/DAY 21928 3 MG FILM-COATED TABLET QD
126444542 12644454 3 SS CHANTIX VARENICLINE TARTRATE 1 4 MG, 1X/DAY 21928 4 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126444542 12644454 1 Smoking cessation therapy

Outcome of event

Event ID CASEID OUTC COD
126444542 12644454 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126444542 12644454 Depression
126444542 12644454 Intentional product use issue
126444542 12644454 Prescribed overdose
126444542 12644454 Suicidal ideation
126444542 12644454 Withdrawal syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126444542 12644454 1 2007 2007 0