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
104204511 10420451 1 I 201404 20140506 20140701 20140701 PER 100067129 FOREST 87.00 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
104204511 10420451 1 PS LINZESS LINACLOTIDE 1 ORAL 1 IN 2 D, D D 202811 145 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104204511 10420451 1 Constipation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104204511 10420451 Gastrointestinal sounds abnormal

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

Event ID CASEID RPSR COD
104204511 10420451 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
104204511 10420451 1 20140403 20140416 0
104204511 10420451 1 20140417 0