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
126354551 12635455 1 I 201607 20160725 20160808 20160808 EXP NL-JNJFOC-20160801074 JOHNSON AND JOHNSON 36.50 YR A F Y 58.00000 KG 20160808 CN NL NL

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
126354551 12635455 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown N U 19835 FILM COATED TABLET
126354551 12635455 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown N U 19835 10 MG FILM COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126354551 12635455 2 Seasonal allergy

Outcome of event

Event ID CASEID OUTC COD
126354551 12635455 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126354551 12635455 Abdominal pain
126354551 12635455 Aphonia
126354551 12635455 Asthenia
126354551 12635455 Diarrhoea
126354551 12635455 Dizziness
126354551 12635455 Dry mouth
126354551 12635455 Ear pain
126354551 12635455 Fatigue
126354551 12635455 Headache
126354551 12635455 Insomnia
126354551 12635455 Loss of consciousness
126354551 12635455 Malaise
126354551 12635455 Micturition disorder
126354551 12635455 Seizure
126354551 12635455 Somnolence
126354551 12635455 Tachycardia
126354551 12635455 Vision blurred

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
126354551 12635455 2 20160720 20160721 0