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
126741321 12674132 1 I 20160811 20160811 20160822 20160822 EXP PHHY2016BR113689 NOVARTIS 53.67 YR F Y 63.00000 KG 20160822 CN BR BR

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
126741321 12674132 1 PS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral (28 TABLETS) (320 MG) U 20818 TABLET
126741321 12674132 2 SS DIOVAN VALSARTAN 1 Oral 80 MG, UNK 0 80 MG TABLET
126741321 12674132 3 SS DIOVAN VALSARTAN 1 Oral 320 MG, (28 TABLETS) 0 320 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126741321 12674132 1 Hypertension
126741321 12674132 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126741321 12674132 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126741321 12674132 Blood potassium decreased
126741321 12674132 Cardiovascular disorder
126741321 12674132 Cerebrovascular accident
126741321 12674132 Drug ineffective
126741321 12674132 Gastrooesophageal reflux disease
126741321 12674132 Headache
126741321 12674132 Hypertension
126741321 12674132 Labyrinthitis
126741321 12674132 Pain
126741321 12674132 Palpitations

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

no results found

Therapies reported

no results found