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
125997271 12599727 1 I 20160609 20160727 20160727 PER US-SA-2016SA110394 AVENTIS 0.00 A F Y 66.68000 KG 20160727 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
125997271 12599727 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Oral UNKNOWN 19908 5 MG FILM-COATED TABLET
125997271 12599727 2 SS AMBIEN ZOLPIDEM TARTRATE 1 Oral UNKNOWN 19908 10 MG FILM-COATED TABLET
125997271 12599727 3 C PREMARIN ESTROGENS, CONJUGATED 1 Unknown 0 1.25 MG TABLET
125997271 12599727 4 C TOVIAZ FESOTERODINE FUMARATE 1 Unknown 0 4 MG TABLET QD
125997271 12599727 5 C TOVIAZ FESOTERODINE FUMARATE 1 Unknown DOSE INCREASED 0 8 MG TABLET QD
125997271 12599727 6 C TOVIAZ FESOTERODINE FUMARATE 1 Unknown DOSE INCREASED 0 4 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125997271 12599727 3 Hyperhidrosis
125997271 12599727 4 Bladder disorder
125997271 12599727 5 Bladder disorder
125997271 12599727 6 Bladder disorder

Outcome of event

Event ID CASEID OUTC COD
125997271 12599727 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125997271 12599727 Emotional distress
125997271 12599727 Loss of consciousness

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

no results found

Therapies reported

no results found