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
125417951 12541795 1 I 20150913 20151022 20160708 20160708 EXP TR-BAYER-2015-451271 BAYER 33.00 YR A M Y 0.00000 20160708 CN TR TR

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
125417951 12541795 1 PS LEVITRA VARDENAFIL HYDROCHLORIDE TRIHYDRATE 1 10 MG, ONCE 200179 10 MG MODIFIED-RELEASE TABLET 1X
125417951 12541795 2 SS CIALIS TADALAFIL 1 5 MG, ONCE 0 5 MG 1X
125417951 12541795 3 C PRANTAL DIPHEMANIL 1 600 MG, UNK 0 600 MG
125417951 12541795 4 C EUTHYROX LEVOTHYROXINE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125417951 12541795 1 Erectile dysfunction
125417951 12541795 4 Goitre

Outcome of event

Event ID CASEID OUTC COD
125417951 12541795 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125417951 12541795 Diarrhoea
125417951 12541795 Hyperhidrosis
125417951 12541795 Insomnia
125417951 12541795 Palpitations
125417951 12541795 Product use issue
125417951 12541795 Unevaluable event
125417951 12541795 Visual impairment

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
125417951 12541795 1 20150913 0
125417951 12541795 2 20150913 0
125417951 12541795 3 201509 0