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
125882421 12588242 1 I 20160427 20160725 20160725 PER US-JNJFOC-20160426159 JANSSEN 0.00 Y 0.00000 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
125882421 12588242 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown U U 19835 UNSPECIFIED
125882421 12588242 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown U U 19835 UNSPECIFIED
125882421 12588242 3 C CLARITIN LORATADINE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125882421 12588242 2 Product used for unknown indication
125882421 12588242 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125882421 12588242 Agitation
125882421 12588242 Alopecia
125882421 12588242 Cough
125882421 12588242 Drug ineffective
125882421 12588242 Feeling of despair
125882421 12588242 Oropharyngeal pain
125882421 12588242 Respiration abnormal
125882421 12588242 Somnolence
125882421 12588242 Upper-airway cough syndrome

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

no results found

Therapies reported

no results found