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
120909572 12090957 2 F 20160721 20160218 20160803 EXP KR-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-09592GL BOEHRINGER INGELHEIM SEONG S,YOON Y,LIM M. SERIOUS ADVERSE EVENTS DURING CLINICAL TRIAL FOR PHARMACOKINETIC INTERACTION BETWEEN TELMISARTAN AND CHLORTHALIDONE IN HEALTHY KOREAN SUBJECTS: A CASE REPORT. TRANSLATIONAL AND CLINICAL PHARMACOLOGY 2015 DEC 15;23 (2):46-48. 36.00 YR M Y 0.00000 20160803 OT COUNTRY NOT SPECIFIED KR

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
120909572 12090957 1 PS MICARDIS TELMISARTAN 1 Oral 80 MG Y 20850 80 MG QD
120909572 12090957 2 SS CHLORTHALIDONE. CHLORTHALIDONE 1 Oral 25 MG U 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120909572 12090957 1 Product used for unknown indication
120909572 12090957 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120909572 12090957 HO
120909572 12090957 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120909572 12090957 Blood potassium decreased
120909572 12090957 Condition aggravated
120909572 12090957 Drug interaction
120909572 12090957 Electrocardiogram QT prolonged
120909572 12090957 Gastrooesophageal reflux disease
120909572 12090957 Heart rate abnormal
120909572 12090957 Hypokalaemia
120909572 12090957 Nausea
120909572 12090957 Reflux gastritis
120909572 12090957 Syncope
120909572 12090957 Vomiting

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

no results found

Therapies reported

no results found