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
124751512 12475151 2 F 20160912 20160617 20160915 PER US-PFIZER INC-2016287570 PFIZER 63.00 YR F Y 0.00000 20160915 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
124751512 12475151 1 PS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, DAILY (EVERYDAY) U 4782 .3 MG TABLET
124751512 12475151 2 SS AMOXICILLIN. AMOXICILLIN 1 UNK U 0
124751512 12475151 3 SS CARDIZEM DILTIAZEM HYDROCHLORIDE 1 120 MG, UNK U 0 120 MG
124751512 12475151 4 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 60 MG, UNK U 0 60 MG
124751512 12475151 5 SS IMITREX SUMATRIPTAN SUCCINATE 1 50 MG, UNK U 0 50 MG
124751512 12475151 6 SS SYNTHROID LEVOTHYROXINE SODIUM 1 UNK U 0
124751512 12475151 7 SS TOPAMAX TOPIRAMATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124751512 12475151 1 Hormone replacement therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124751512 12475151 Drug hypersensitivity

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

no results found

Therapies reported

no results found