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
127133591 12713359 1 I 201601 20160205 20160902 20160902 PER US-ZYDUS-010315 ZYDUS PHARM 59.00 YR M Y 0.00000 20160902 PH 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
127133591 12713359 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Oral MR8725 78226 10 MG TABLET
127133591 12713359 2 C TRAMADOL/TRAMADOL HYDROCHLORIDE 2 U 0
127133591 12713359 3 C LOSARTAN/LOSARTAN POTASSIUM 2 U 0 25 MG
127133591 12713359 4 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 U 0 40 MG
127133591 12713359 5 C SILDENAFIL/SILDENAFIL CITRATE 2 U 0 20 MG
127133591 12713359 6 C TAMSULOSIN/TAMSULOSIN HYDROCHLORIDE 2 U 0 .4 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127133591 12713359 1 Hypertension
127133591 12713359 2 Pain
127133591 12713359 3 Hypertension
127133591 12713359 4 Gastrooesophageal reflux disease
127133591 12713359 5 Erectile dysfunction

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127133591 12713359 Drug ineffective Drug ineffective
127133591 12713359 Headache Headache

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
127133591 12713359 1 20160120 0
127133591 12713359 2 201601 0
127133591 12713359 3 201507 0
127133591 12713359 4 201512 0
127133591 12713359 5 201512 0