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
127391731 12739173 1 I 201512 20151208 20160913 20160913 PER US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-10460-2015 RECKITT BENCKISER 78.00 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
127391731 12739173 1 PS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Oral 2400 MG, SINGLE U BM617 0 2400 MG TABLET
127391731 12739173 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown UNK U 0
127391731 12739173 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown UNK U 0
127391731 12739173 4 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127391731 12739173 1 Cough
127391731 12739173 2 Product used for unknown indication
127391731 12739173 3 Product used for unknown indication
127391731 12739173 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127391731 12739173 Accidental overdose
127391731 12739173 Insomnia

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
127391731 12739173 1 20151208 0