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
126160033 12616003 3 F 201607 20160826 20160802 20160901 EXP JP-PFIZER INC-2016367273 PFIZER 66.00 YR M Y 169.00000 KG 20160901 CN JP JP

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
126160033 12616003 1 PS TOVIAZ FESOTERODINE FUMARATE 1 Oral 4 MG, DAILY Y 22030 4 MG PROLONGED-RELEASE TABLET
126160033 12616003 2 SS TOVIAZ FESOTERODINE FUMARATE 1 8 MG, 1X/DAY (AT NIGHT) Y 22030 8 MG PROLONGED-RELEASE TABLET QD
126160033 12616003 3 C LOSARHYD HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM 1 0
126160033 12616003 4 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126160033 12616003 5 C ATORVASTATIN ATORVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126160033 12616003 1 Hypertonic bladder

Outcome of event

Event ID CASEID OUTC COD
126160033 12616003 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126160033 12616003 Condition aggravated
126160033 12616003 Drug ineffective
126160033 12616003 Dry mouth
126160033 12616003 Dysphagia
126160033 12616003 Dysphonia
126160033 12616003 Hypotonic urinary bladder
126160033 12616003 Lip dry
126160033 12616003 Thirst
126160033 12616003 Urinary retention

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
126160033 12616003 1 20160726 20160726 0
126160033 12616003 2 20160727 201607 0