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
126891201 12689120 1 I 20160811 20160826 20160826 PER US-BAYER-2016-158689 BAYER 59.00 YR A F Y 61.22000 KG 20160826 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
126891201 12689120 1 PS CLARITIN-D 24 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 Oral 1 DF, QD 20470 1 DF PROLONGED-RELEASE TABLET QD
126891201 12689120 2 SS CHILDREN CLARITIN ALLERGY LORATADINE 1 Oral 1 DF, QD 0 1 DF SYRUP QD
126891201 12689120 3 C RILUZOLE. RILUZOLE 1 UNK 0
126891201 12689120 4 C LEXAPRO ESCITALOPRAM OXALATE 1 UNK 0
126891201 12689120 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
126891201 12689120 6 C MOBIC MELOXICAM 1 0
126891201 12689120 7 C ALBUTEROL. ALBUTEROL 1 0
126891201 12689120 8 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126891201 12689120 Drug ineffective
126891201 12689120 Drug prescribing error
126891201 12689120 Product use issue
126891201 12689120 Therapeutic response unexpected
126891201 12689120 Wrong technique in product usage process

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
126891201 12689120 1 201608 0
126891201 12689120 2 201608 0