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
125658222 12565822 2 F 20160726 20160718 20160803 EXP PHHY2016MX095315 NOVARTIS 0.00 F Y 0.00000 20160803 CN MX MX

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
125658222 12565822 1 PS DIOVAN VALSARTAN 1 Unknown 4 DF (160 MG), QD (EVERY 4 HOURS) 1 YEAR APPROX 1526671 21283 4 DF TABLET QD
125658222 12565822 2 SS DIOVAN VALSARTAN 1 Unknown 4 DF, QD (160 MG) 21283 4 DF TABLET QD
125658222 12565822 3 C RANISEN 2 Unknown 150 MG, UNK U 0 150 MG
125658222 12565822 4 C BETOPTIC S BETAXOLOL HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125658222 12565822 1 Hypertension
125658222 12565822 3 Product used for unknown indication
125658222 12565822 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125658222 12565822 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125658222 12565822 Blood pressure increased
125658222 12565822 Drug prescribing error
125658222 12565822 Hypersensitivity
125658222 12565822 Inappropriate schedule of drug administration
125658222 12565822 Ocular hyperaemia
125658222 12565822 Ocular hypertension

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

no results found

Therapies reported

no results found