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
126180641 12618064 1 I 20160715 20160803 20160803 PER US-JNJFOC-20160713979 JANSSEN 67.00 YR E F Y 82.56000 KG 20160803 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
126180641 12618064 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN 19835 TABLET
126180641 12618064 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N UNKNOWN 19835 10 MG TABLET QD
126180641 12618064 3 C MAGNESIUM MAGNESIUM 1 Unknown 0 UNSPECIFIED
126180641 12618064 4 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0 UNSPECIFIED
126180641 12618064 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180641 12618064 2 Multiple allergies
126180641 12618064 3 Nutritional supplementation
126180641 12618064 4 Abdominal pain upper
126180641 12618064 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180641 12618064 Drug administration error
126180641 12618064 Drug ineffective

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

no results found

Therapies reported

no results found