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
127861571 12786157 1 I 2016 20160601 20160927 20160927 PER US-FRI-1000085186 ALLERGAN 62.21 YR M Y 106.59000 KG 20160927 CN 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
127861571 12786157 1 PS LINZESS LINACLOTIDE 1 Oral 290 ?G, UNK D A474324 202811 290 UG CAPSULE
127861571 12786157 2 SS LINZESS LINACLOTIDE 1 Oral 290 ?G, QD D A474401 202811 290 UG CAPSULE QD
127861571 12786157 3 SS DULCOLAX NOS BISACODYL OR DOCUSATE SODIUM 1 TOOK 3 DULCOLAX D 0
127861571 12786157 4 C XANAX ALPRAZOLAM 1 Oral UNK U 0
127861571 12786157 5 C XANAX ALPRAZOLAM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127861571 12786157 1 Gastrointestinal motility disorder
127861571 12786157 4 Sleep disorder
127861571 12786157 5 Anxiety

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127861571 12786157 Abdominal pain
127861571 12786157 Diarrhoea
127861571 12786157 Gallbladder pain
127861571 12786157 Gastrointestinal disorder
127861571 12786157 Gastrointestinal pain
127861571 12786157 Hepatic pain
127861571 12786157 Intentional product misuse
127861571 12786157 Liver disorder
127861571 12786157 Malaise
127861571 12786157 Off label use

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127861571 12786157 1 20160329 201605 0
127861571 12786157 2 201605 0
127861571 12786157 3 20160617 0