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
125864461 12586446 1 I 20160708 20160712 20160725 20160725 PER US-BAYER-2016-136763 BAYER 86.00 YR E F Y 74.83000 KG 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
125864461 12586446 1 PS CLARITIN REDITABS LORATADINE 1 Oral 1 DF, QD CDMO19H 20704 1 DF ORODISPERSIBLE TABLET QD
125864461 12586446 2 SS CLARITIN LORATADINE 1 UNK UNK 0 TABLET
125864461 12586446 3 C ATENOLOL. ATENOLOL 1 UNK UNK 0
125864461 12586446 4 C ASPIRIN. ASPIRIN 1 UNK UNK 0
125864461 12586446 5 C NAPROXEN. NAPROXEN 1 UNK UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125864461 12586446 1 Rash
125864461 12586446 2 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125864461 12586446 Drug ineffective
125864461 12586446 Off label use

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
125864461 12586446 1 20160708 0