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
127394561 12739456 1 I 20160413 20160413 20160913 20160913 PER US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-85233-2016 RECKITT BENCKISER 60.72 YR F Y 0.00000 20160913 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
127394561 12739456 1 PS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Unknown UNK U U 0 TABLET
127394561 12739456 2 SS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Unknown 1200 MG, SINGLE U U 0 1200 MG TABLET
127394561 12739456 3 SS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Unknown 1200 MG, SINGLE U U 0 1200 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127394561 12739456 1 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127394561 12739456 Dizziness
127394561 12739456 Product use issue

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
127394561 12739456 1 20160409 0
127394561 12739456 2 20160412 0
127394561 12739456 3 20160413 0