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
126253861 12625386 1 I 20160725 20160805 20160805 PER US-BAYER-2016-145043 BAYER 77.00 YR E M Y 0.00000 20160805 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
126253861 12625386 1 PS CLARITIN-D 24 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 Oral 1 DF, UNK CVM081K 20470 1 DF PROLONGED-RELEASE TABLET
126253861 12625386 2 SS CLARITIN-D 12 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 Oral 1 DF, UNK 20470 1 DF PROLONGED-RELEASE TABLET
126253861 12625386 3 SS BAYER GENUINE ASPIRIN ASPIRIN 1 0 FILM-COATED TABLET
126253861 12625386 4 C ALEVE NAPROXEN SODIUM 1 0 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126253861 12625386 1 Dyspnoea
126253861 12625386 2 Dyspnoea
126253861 12625386 3 Product used for unknown indication
126253861 12625386 4 Back pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126253861 12625386 Product use issue
126253861 12625386 Product used for unknown indication

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
126253861 12625386 1 2010 0