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
124427473 12442747 3 F 20160711 20160607 20160718 EXP PHHY2016BR076812 NOVARTIS 0.00 F Y 70.00000 KG 20160717 MD 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
124427473 12442747 1 PS DIOVAN VALSARTAN 1 Oral 80 MG, QD (1 TABLET AT 8 AM) (28 TABLETS) U 1526552 21283 80 MG TABLET QD
124427473 12442747 2 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD U 0 75 MG TABLET QD
124427473 12442747 3 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD Y 0 75 MG TABLET QD
124427473 12442747 4 C ANGIPRESS ATENOLOL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124427473 12442747 1 Hypertension
124427473 12442747 2 Thrombosis prophylaxis
124427473 12442747 3 Thrombosis prophylaxis
124427473 12442747 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124427473 12442747 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124427473 12442747 Anxiety
124427473 12442747 Blindness unilateral
124427473 12442747 Blood pressure increased
124427473 12442747 Cerebrovascular accident
124427473 12442747 Ear disorder
124427473 12442747 Hypotension
124427473 12442747 Retinal vascular thrombosis

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

no results found

Therapies reported

no results found