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
113232452 11323245 2 F 201411 20141126 20150730 20160729 EXP US-MYLANLABS-2014M1011979 MYLAN 0.00 Y 0.00000 20160729 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
113232452 11323245 1 PS Levothyroxine Sodium Tablets, USP LEVOTHYROXINE SODIUM 1 Oral 75 ?G, QD Y Y 3056289 76187 75 UG TABLET QD
113232452 11323245 2 SS Levothyroxine Sodium Tablets, USP LEVOTHYROXINE SODIUM 1 Oral 75 ?G, QD Y Y 3056289 76187 75 UG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113232452 11323245 1 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
113232452 11323245 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113232452 11323245 Arrhythmia
113232452 11323245 Chest discomfort
113232452 11323245 Dyspnoea
113232452 11323245 Fatigue
113232452 11323245 Fluid retention
113232452 11323245 Headache
113232452 11323245 Insomnia
113232452 11323245 Malaise
113232452 11323245 Pain in extremity
113232452 11323245 Reaction to drug excipients

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
113232452 11323245 1 201411 201411 0
113232452 11323245 2 201411 201412 0