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
104204571 10420457 1 I 201405 20140509 20140701 20140701 PER 1000067242 FOREST 62.00 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
104204571 10420457 1 PS LINZESS LINACLOTIDE 1 ORAL N D 202811 145 UG QD
104204571 10420457 2 SS LINZESS LINACLOTIDE 1 ORAL APPROXIMATELY 1/4 OF CAPSULE Y D 0
104204571 10420457 4 C IMITREX SUMATRIPTANSUMATRIPTAN SUCCINATE 1 0
104204571 10420457 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104204571 10420457 1 Irritable bowel syndrome
104204571 10420457 2 Irritable bowel syndrome

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104204571 10420457 Diarrhoea
104204571 10420457 Intentional product misuse

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

Event ID CASEID RPSR COD
104204571 10420457 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
104204571 10420457 1 201405 201405 0
104204571 10420457 2 201405 201405 0
104204571 10420457 2 201405 0