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
122821052 12282105 2 F 20160726 20160419 20160817 PER US-PFIZER INC-2016208736 PFIZER 78.00 YR F Y 0.00000 20160817 MD 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
122821052 12282105 1 PS TOVIAZ FESOTERODINE FUMARATE 1 Oral 8 MG, 1X/DAY Y F10258730 22030 8 MG MODIFIED-RELEASE TABLET QD
122821052 12282105 2 SS TOVIAZ FESOTERODINE FUMARATE 1 Y 22030 MODIFIED-RELEASE TABLET
122821052 12282105 3 C LASIX FUROSEMIDE 1 40 MG, 1X/DAY 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122821052 12282105 1 Bladder disorder
122821052 12282105 2 Incontinence

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122821052 12282105 Constipation
122821052 12282105 Dry mouth
122821052 12282105 Dry throat
122821052 12282105 Eye swelling
122821052 12282105 Eyelid oedema
122821052 12282105 Fluid retention
122821052 12282105 Swelling face
122821052 12282105 Weight increased

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
122821052 12282105 1 20160410 0