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
124967212 12496721 2 F 20160628 20160624 20160705 EXP JP-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-39144NB BOEHRINGER INGELHEIM NAKANISHI M,KANAYAMA K,TAKAHASHI K,HAYASHI H,KOIDE S,HASEGAWA M,ET AL. A CASE OF END-STAGE RENAL FAILURE THAT THE DECREASE OF BLOOD PRESSURE WAS IMPROVED BY SIGNIFICANT IMPROVEMENT OF METABOLIC ACIDOSIS WITH BLOOD DIALYSIS. JOURNAL OF THE JAPANESE SOCIETY FOR DIALYSIS THERAPY 2016 MAY;49(S1):9.4. 66.00 YR M Y 0.00000 20160706 OT COUNTRY NOT SPECIFIED JP

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
124967212 12496721 1 PS MICARDIS TELMISARTAN 1 Oral 40 MG N 20850 40 MG TABLET QD
124967212 12496721 2 C CILNIDIPINE CILNIDIPINE 1 Oral 2.8571 MG N 0 20 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124967212 12496721 1 Product used for unknown indication
124967212 12496721 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124967212 12496721 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124967212 12496721 Blood pressure decreased
124967212 12496721 Cardiomegaly
124967212 12496721 Metabolic acidosis
124967212 12496721 Oedema

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

no results found

Therapies reported

no results found