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
104204581 10420458 1 I 201404 20140513 20140701 20140701 PER 1000067324 FOREST 89.00 YR F N 0.00000 20140612 N CN 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
104204581 10420458 1 PS LINZESS LINACLOTIDE 1 ORAL 290 MCG ( 290 MCG, 1 N 1 D) ORAL D D 202811 290 UG 1X
104204581 10420458 3 C PROZAC ( FLUOXETINE HYDROCHLORIDE) (FLUOXETINE HYDROCHLORIDE) 2 0
104204581 10420458 5 C PROTONIX ( PANTOPRAZOLE SODIUM SESQUIHYDRATE) (PANTOPRAZOLE SODIUM SESQUIHYDRATE) 2 0
104204581 10420458 7 C VICODIN ( HYDROCODONE, ACETAMINOPHEN) (HYDROCODONE, ACETAMINOPHEN) 2 0
104204581 10420458 9 C AMBIEN ( ZOLPIDEM TARTRATE) (ZOLPIDEM TARTRATE) 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104204581 10420458 1 Constipation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104204581 10420458 Cold sweat

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

Event ID CASEID RPSR COD
104204581 10420458 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
104204581 10420458 1 20140404 0