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
126908231 12690823 1 I 201508 20160817 20160826 20160826 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-54101BP BOEHRINGER INGELHEIM 69.87 YR F Y 0.00000 20160826 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
126908231 12690823 1 PS MICARDIS TELMISARTAN 1 Oral DOSE PER APPLICATION: 40MG/12.5MG; DAILY DOSE:40MG/12.5MG N 20850 QD
126908231 12690823 2 SS MICARDIS TELMISARTAN 1 Oral DOSE PER APPLICATION: 40MG/12.5MG DAILY DOSE: 22.86/7.14MG N 20850
126908231 12690823 3 C LEVOTHYROXIN LEVOTHYROXINE 1 Oral 112 MCG 0 112 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126908231 12690823 1 Hypertension
126908231 12690823 3 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126908231 12690823 Blood uric acid increased
126908231 12690823 Dehydration
126908231 12690823 Dry skin

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
126908231 12690823 1 2014 201512 0
126908231 12690823 2 201512 0
126908231 12690823 3 1986 0