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
127288771 12728877 1 I 20160131 20160909 20160909 PER US-APOTEX-2016AP006370 APOTEX 0.00 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
127288771 12728877 1 PS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Unknown Y 90790 TABLET
127288771 12728877 2 SS DILTIAZEM HYDROCHLORIDE. DILTIAZEM HYDROCHLORIDE 1 Unknown 1 CAPSULE DAILY Y 0 1 DF CAPSULE
127288771 12728877 3 SS LOTREL AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE 1 Unknown UNK Y 0
127288771 12728877 4 SS TRIAMTERENE AND HYDROCHLOROTHIAZID HYDROCHLOROTHIAZIDETRIAMTERENE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127288771 12728877 1 Hypertension
127288771 12728877 2 Hypertension
127288771 12728877 3 Hypertension
127288771 12728877 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127288771 12728877 Blood pressure increased
127288771 12728877 Drug ineffective
127288771 12728877 Pruritus
127288771 12728877 Urticaria

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found