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
126812081 12681208 1 I 20160729 20160823 20160824 20160824 EXP PHHY2016FR115744 NOVARTIS 53.00 YR F Y 0.00000 20160824 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
126812081 12681208 1 PS TAREG VALSARTAN 1 Unknown 80 MG, UNK 20665 80 MG CAPSULE
126812081 12681208 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 60 MG, QD 0 60 MG GASTRO-RESISTANT CAPSULES QD
126812081 12681208 3 SS BISOPROLOL BISOPROLOL 1 Unknown UNK 0
126812081 12681208 4 SS TERCIAN CYAMEMAZINE 1 Unknown UNK 0
126812081 12681208 5 SS ZOPICLONE ZOPICLONE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126812081 12681208 1 Hypertension
126812081 12681208 2 Depression
126812081 12681208 3 Hypertension
126812081 12681208 4 Depression
126812081 12681208 5 Insomnia

Outcome of event

Event ID CASEID OUTC COD
126812081 12681208 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126812081 12681208 Hypochloraemia
126812081 12681208 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
126812081 12681208 2 201501 0