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
125573251 12557325 1 I 2016 20160630 20160714 20160714 EXP US-GLAXOSMITHKLINE-US2016GSK094332 GLAXOSMITHKLINE 44.00 YR F Y 0.00000 20160714 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
125573251 12557325 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 2 DF, BID U 18703 2 DF CAPSULE BID
125573251 12557325 2 SS Morphine MORPHINE 1 U 0
125573251 12557325 3 SS XELJANZ TOFACITINIB CITRATE 1 UNK U 0
125573251 12557325 4 C ECOTRIN ASPIRIN 1 U 0
125573251 12557325 5 C FIORICET ACETAMINOPHENBUTALBITALCAFFEINE 1 U 0
125573251 12557325 6 C FLONASE FLUTICASONE PROPIONATE 1 U 0
125573251 12557325 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 U 0
125573251 12557325 8 C NITROGLYCERIN. NITROGLYCERIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125573251 12557325 1 Abdominal pain
125573251 12557325 2 Product used for unknown indication
125573251 12557325 3 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125573251 12557325 Abdominal pain upper
125573251 12557325 Drug hypersensitivity
125573251 12557325 Drug ineffective

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
125573251 12557325 1 2016 0
125573251 12557325 3 20160527 0