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
125297292 12529729 2 F 201606 20160915 20160706 20160923 EXP US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-87648-2016 RECKITT BENCKISER 73.63 YR F Y 0.00000 20160923 OT 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
125297292 12529729 1 PS MUCINEX GUAIFENESIN 1 Unknown 600 MG, BID (EVERY 12 HOURS) Y U 0 600 MG TABLET
125297292 12529729 2 SS ANTIVERT /00007101/ MECLIZINE MONOHYDROCHLORIDENIACIN 1 Unknown UNK Y U 0
125297292 12529729 3 C ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125297292 12529729 1 Product used for unknown indication
125297292 12529729 2 Vertigo
125297292 12529729 3 Sinusitis bacterial

Outcome of event

Event ID CASEID OUTC COD
125297292 12529729 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125297292 12529729 Confusional state
125297292 12529729 Headache
125297292 12529729 Product use issue
125297292 12529729 Vision blurred

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
125297292 12529729 1 201606 20160630 0
125297292 12529729 2 201606 201606 0
125297292 12529729 3 20160227 0