The Safety Rates Drug Report

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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
126069101 12606910 1 I 20160719 20160729 20160729 EXP CZ-TEVA-679198ISR TEVA SIMCIKOVA T,TABORSKY P. NEOBVYKLA MANIFESTACE NEZADOUCIHO UCINKU PIOGLITAZONU / UNUSUAL MANIFESTATION OF PIOGLITAZONE ADVERSE EVENT. AKTUALITY V NEFROLOGII. 2016 JAN 01;1/2016:37-38. 63.00 YR M Y 0.00000 20160729 MD CZ CZ

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
126069101 12606910 1 PS PIOGLITAZONE. PIOGLITAZONE 1 Oral Y 77210 TABLET
126069101 12606910 2 SS INDAPAMIDE. INDAPAMIDE 1 Oral Y 0 TABLET
126069101 12606910 3 C PERINDOPRIL PERINDOPRIL 1 Oral 0 TABLET
126069101 12606910 4 C INSULIN INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126069101 12606910 1 Diabetes mellitus
126069101 12606910 2 Hypertension
126069101 12606910 3 Hypertension
126069101 12606910 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126069101 12606910 OT
126069101 12606910 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126069101 12606910 Haematocrit decreased
126069101 12606910 Hyperglycaemia
126069101 12606910 Hypokalaemia

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

no results found

Therapies reported

no results found