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
125890571 12589057 1 I 20160622 20160624 20160725 20160725 PER US-JNJFOC-20160624355 JANSSEN 68.00 YR E M Y 86.18000 KG 20160725 CN US US

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
125890571 12589057 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474651 19835 TABLET
125890571 12589057 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 10 MG, 1 TABLET A DAY N 474651 19835 10 MG TABLET QD
125890571 12589057 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown DAILY 0 12.5 MG UNSPECIFIED
125890571 12589057 4 C BABY ASPIRIN ASPIRIN 1 Unknown DAILY 0 81 MG UNSPECIFIED
125890571 12589057 5 C ATORVASTATIN ATORVASTATIN 1 Unknown DAILY 0 40 MG UNSPECIFIED
125890571 12589057 6 C METOPROLOL. METOPROLOL 1 Unknown 0 25 MG UNSPECIFIED BID
125890571 12589057 7 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown DAILY 0 40 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125890571 12589057 2 Multiple allergies
125890571 12589057 3 Diuretic therapy
125890571 12589057 4 Cardiac disorder
125890571 12589057 5 Blood cholesterol increased
125890571 12589057 6 Hypertension
125890571 12589057 7 Hyperchlorhydria

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125890571 12589057 Pruritus
125890571 12589057 Rash

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
125890571 12589057 2 20160622 20160623 0