The Safety Rates Drug Report

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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
127388631 12738863 1 I 20151001 20160913 20160913 PER US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-08284-2015 RECKITT BENCKISER 0.00 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
127388631 12738863 1 PS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Unknown 1200 MG, SINGLE 1200 MG U U BL682 0 1200 MG TABLET
127388631 12738863 2 SS MUCINEX GUAIFENESIN 1 Unknown 600 MG, BID U 0 600 MG TABLET
127388631 12738863 3 SS MUCINEX GUAIFENESIN 1 Unknown 600 MG, QD U 0 600 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127388631 12738863 1 Product used for unknown indication
127388631 12738863 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127388631 12738863 Dyspnoea
127388631 12738863 Incorrect drug administration duration
127388631 12738863 Nausea
127388631 12738863 Nervousness

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
127388631 12738863 1 20150929 0