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
127275701 12727570 1 I 20160727 20160830 20160909 20160909 PER PHHY2016US124124 SANDOZ 67.00 YR F Y 0.00000 20160909 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
127275701 12727570 1 SS DICLOFENAC SODIUM. DICLOFENAC SODIUM 1 Unknown 2 G, BID Y U 0 2 G EMULGEL BID
127275701 12727570 2 PS CARVEDILOL. CARVEDILOL 1 Unknown 6.25 MG, BID Y 78227 6.25 MG TABLET BID
127275701 12727570 3 SS CARVEDILOL. CARVEDILOL 1 Unknown 6.25 MG, QD Y 78227 6.25 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127275701 12727570 1 Arthritis
127275701 12727570 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127275701 12727570 Dizziness
127275701 12727570 Emergency care examination
127275701 12727570 Fall
127275701 12727570 Heart rate irregular
127275701 12727570 Muscle injury
127275701 12727570 Troponin 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
127275701 12727570 1 20160720 0