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
97481843 9748184 3 F 20160725 20131212 20160801 PER US-PFIZER INC-2013353339 PFIZER 63.00 YR F Y 0.00000 20160801 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
97481843 9748184 1 PS AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 UNK U 19787
97481843 9748184 2 SS CHANTIX VARENICLINE TARTRATE 1 UNK U 21928 FILM-COATED TABLET
97481843 9748184 3 SS SULFUR. SULFUR 1 UNK U 0
97481843 9748184 4 SS DARVOCET-N 100 ACETAMINOPHENPROPOXYPHENE NAPSYLATE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
97481843 9748184 Drug hypersensitivity

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

no results found

Therapies reported

no results found