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
123863682 12386368 2 F 2014 20160920 20160519 20160929 EXP BR-ABBVIE-16P-020-1632347-00 ABBVIE 0.00 F Y 0.00000 20160929 CN COUNTRY NOT SPECIFIED BR

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
123863682 12386368 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown Y UNKNOWN 21402
123863682 12386368 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown Y UNKNOWN 21402

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123863682 12386368 1 Autoimmune thyroiditis

Outcome of event

Event ID CASEID OUTC COD
123863682 12386368 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123863682 12386368 Depression
123863682 12386368 Diabetes mellitus
123863682 12386368 Metabolic surgery
123863682 12386368 Weight increased

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
123863682 12386368 1 2006 0