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
125931871 12593187 1 I 201509 20160510 20160726 20160726 PER US-ABBVIE-16P-163-1626617-00 ABBVIE 66.13 YR F Y 0.00000 20160726 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
125931871 12593187 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y 21402 TABLET QOD
125931871 12593187 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN,UNKNOWN 21402 TABLET QD
125931871 12593187 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN,UNKNOWN 21402 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125931871 12593187 1 Hypothyroidism
125931871 12593187 2 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125931871 12593187 Agitation
125931871 12593187 Asthenia
125931871 12593187 Blood thyroid stimulating hormone decreased
125931871 12593187 Fatigue
125931871 12593187 Illogical thinking
125931871 12593187 Product quality issue
125931871 12593187 Treatment noncompliance

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
125931871 12593187 1 201509 20160510 0
125931871 12593187 2 201509 0
125931871 12593187 3 20160510 0