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
104204481 10420448 1 I 20140516 20140523 20140701 20140701 PER 1000067626 FOREST 53.00 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
104204481 10420448 1 PS LINZESS LINACLOTIDE 1 ORAL D D A370686 201508 202811 290 UG QD
104204481 10420448 2 C MIRALAX (POLYETHYL ENE GLYCOL 335020 2 0
104204481 10420448 4 C HUMALOG(INSULIN LISPRO) 2 0
104204481 10420448 6 C PROAIR HFA(SALBUTAMOL SULFATE) 2 0
104204481 10420448 8 C ESCITALOPRAM(ESCITALOPRAM OXALATE) OXALATE) 2 0
104204481 10420448 10 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 0
104204481 10420448 12 C ALPRAZOLAM. ALPRAZOLAM 1 0
104204481 10420448 14 C AMITRIPTYLINE AMITRIPTYLINE 1 0
104204481 10420448 16 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
104204481 10420448 18 C DILTIAZEM(DILTIAZEM HYDROCHLORIDE) 2 0
104204481 10420448 20 C SYMLIN(PRAMLINTIDE ACETATE) 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104204481 10420448 1 Constipation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104204481 10420448 Abdominal pain
104204481 10420448 Drug effect decreased
104204481 10420448 Flatulence
104204481 10420448 Nausea

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

Event ID CASEID RPSR COD
104204481 10420448 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
104204481 10420448 1 201312 0