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
126763891 12676389 1 I 20160813 0 20160822 20160822 DIR 68.00 YR M N 205.00000 LBS 20160821 N 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
126763891 12676389 1 PS TOVIAZ FESOTERODINE FUMARATE 1 Oral Y D F10242030 20170630 0 17 DF COATED TABLET QD
126763891 12676389 3 C OMEPRAZOLE. OMEPRAZOLE 1 0
126763891 12676389 5 C LOSARTAN. LOSARTAN 1 0
126763891 12676389 7 C ATORVASTATIN ATORVASTATIN 1 0
126763891 12676389 9 C BABY ASPIRIN ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126763891 12676389 1 Hypertonic bladder

Outcome of event

Event ID CASEID OUTC COD
126763891 12676389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126763891 12676389 Constipation
126763891 12676389 Headache
126763891 12676389 Lactose intolerance

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
126763891 12676389 1 20160731 20160816 0