The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6258305 7394360 I 6258305-8 20090630 20090702 DIR 6 YR M N 52 LBS 20090701 CN N N UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6258305 1011846129 PS CHILDREN'S ZYRTEC ALLERGY 1 ORAL 5 ML DAILY PO N N
6258305 1011872867 SS EQUATE ALLERGY RELIEF (CETIRIZINE HCL) 2 ORAL 5 ML DAILY PO N N 20110430

Indications of drugs used

Event ID DRUG SEQ INDI PT
6258305 1011846129 SEASONAL ALLERGY
6258305 1011872867 SEASONAL ALLERGY

Outcome of event

Event ID OUTC COD
6258305 OT

Reactions reported

Event ID PT
6258305 PRURITUS GENERALISED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6258305 1011846129 20090501 20090531
6258305 1011872867 20090601 20090630