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
127029591 12702959 1 I 20160810 20160824 20160831 20160831 EXP CH-SM-2016-06682 CH-GLAXOSMITHKLINE-CH2016123239 GLAXOSMITHKLINE 82.94 YR F Y 75.00000 KG 20160831 PH CH CH

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
127029591 12702959 1 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 35 MG, UNK, 50 MG SINGLE DOSE U 0 35 MG SOLUTION FOR INJECTION
127029591 12702959 2 PS Tavegyl CLEMASTINE FUMARATE 1 Intravenous bolus 4 MG, UNK, 4 MG SINGLE DOSE FOR ABOUT 5 MIN 20925 4 MG
127029591 12702959 3 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous bolus 125 MG, UNK 0 125 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127029591 12702959 1 Allergy prophylaxis
127029591 12702959 2 Allergy prophylaxis
127029591 12702959 3 Allergy prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127029591 12702959 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127029591 12702959 Hypersensitivity

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
127029591 12702959 1 20160810 20160810 0
127029591 12702959 2 20160810 20160810 0
127029591 12702959 3 20160810 20160810 0