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
126148691 12614869 1 I 20160718 20160802 20160802 EXP US-GLAXOSMITHKLINE-US2016GSK111162 GLAXOSMITHKLINE 71.00 YR F Y 0.00000 20160802 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
126148691 12614869 1 PS WELLBUTRIN XL BUPROPION HYDROCHLORIDE 1 Oral 300 MG, QD U 15M020P 18644 300 MG TABLET QD
126148691 12614869 2 SS MUCINEX FAST-MAX DM MAX DEXTROMETHORPHAN HYDROBROMIDEGUAIFENESIN 1 Oral 2 DF, Q4H Y 0 2 DF
126148691 12614869 3 SS MUCINEX FAST-MAX DM MAX DEXTROMETHORPHAN HYDROBROMIDEGUAIFENESIN 1 Y 0
126148691 12614869 4 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 U 0
126148691 12614869 5 C BEE POLLEN BEE POLLEN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126148691 12614869 1 Depression
126148691 12614869 2 Malaise
126148691 12614869 3 Respiratory tract congestion
126148691 12614869 4 Product used for unknown indication
126148691 12614869 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126148691 12614869 Chest discomfort
126148691 12614869 Cough
126148691 12614869 Dizziness Dizziness
126148691 12614869 Headache
126148691 12614869 Malaise
126148691 12614869 Oropharyngeal pain
126148691 12614869 Respiratory tract congestion
126148691 12614869 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
126148691 12614869 1 2012 0