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
126945741 12694574 1 I 20160520 20160826 20160829 20160829 EXP PHHY2016FR118120 NOVARTIS 86.42 YR F Y 0.00000 20160829 OT FR FR

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
126945741 12694574 1 PS EXFORGE AMLODIPINE BESYLATEVALSARTAN 1 Oral 160/10 MG, UNK Y 21990
126945741 12694574 2 SS ALDACTONE SPIRONOLACTONE 1 Oral 50 MG, UNK Y 0 50 MG
126945741 12694574 3 SS LODOZ BISOPROLOL FUMARATEHYDROCHLOROTHIAZIDE 1 Oral 10/6.25 MG, UNK Y 0 FILM-COATED TABLET
126945741 12694574 4 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126945741 12694574 1 Product used for unknown indication
126945741 12694574 2 Product used for unknown indication
126945741 12694574 3 Product used for unknown indication
126945741 12694574 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126945741 12694574 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126945741 12694574 Hyponatraemia

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
126945741 12694574 1 20160520 0
126945741 12694574 2 20160520 0
126945741 12694574 3 20160520 0
126945741 12694574 4 20160520 0