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
126124701 12612470 1 I 2015 20150731 20160801 20160801 PER US-PRINSTON PHARMACEUTICAL INC.-2015PRN00060 PRINSTON PHARMACEUTICAL 71.42 YR F Y 46.26000 KG 20160705 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
126124701 12612470 1 PS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Oral 50 MG, 1X/DAY 100 MG Y 91497 50 MG TABLET QD
126124701 12612470 2 C DILTIAZEM. DILTIAZEM 1 60 MG, 1X/DAY 0 60 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126124701 12612470 1 Tachycardia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126124701 12612470 Abdominal distension
126124701 12612470 Blood pressure decreased
126124701 12612470 Chest discomfort
126124701 12612470 Dyspnoea
126124701 12612470 Fatigue
126124701 12612470 Fluid retention
126124701 12612470 Muscle spasms
126124701 12612470 Pain in extremity
126124701 12612470 Peripheral swelling
126124701 12612470 Presyncope
126124701 12612470 Product substitution issue

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
126124701 12612470 1 20150727 20150731 0
126124701 12612470 2 2002 0