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
125892001 12589200 1 I 20160513 20160725 20160725 PER US-JNJFOC-20160514342 JANSSEN 0.00 F 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
125892001 12589200 1 PS MOTRIN INFANTS IBUPROFEN 1 Oral U U UNK 20603 DROPS
125892001 12589200 2 SS MOTRIN INFANTS IBUPROFEN 1 Oral U U UNK 20603 DROPS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125892001 12589200 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125892001 12589200 Burning sensation
125892001 12589200 Drug administered to patient of inappropriate age
125892001 12589200 Off label use
125892001 12589200 Product taste abnormal

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

no results found

Therapies reported

no results found