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
125105102 12510510 2 F 20160105 20160107 20160629 20160913 PER US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-80851-2016 RECKITT BENCKISER 85.00 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
125105102 12510510 1 PS MUCINEX GUAIFENESIN 1 Unknown UNK 0
125105102 12510510 2 C LABETALOL LABETALOLLABETALOL HYDROCHLORIDE 1 Unknown UNK U 0
125105102 12510510 3 C BUMETANIDE. BUMETANIDE 1 Unknown UNK U 0
125105102 12510510 4 C POTASSIUM POTASSIUM 1 Unknown UNK U 0
125105102 12510510 5 C CALCIUM CALCIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125105102 12510510 1 Cough
125105102 12510510 2 Product used for unknown indication
125105102 12510510 3 Product used for unknown indication
125105102 12510510 4 Product used for unknown indication
125105102 12510510 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125105102 12510510 Diarrhoea

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
125105102 12510510 1 20160105 0