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
125930031 12593003 1 I 201508 20160314 20160726 20160726 PER US-ABBVIE-16P-163-1585096-00 ABBVIE 76.39 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
125930031 12593003 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 50 MCG UNKNOWN 21402 TABLET QD
125930031 12593003 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 75 MCG UNKNOWN 21402 TABLET QD
125930031 12593003 3 C SIMVASTATIN. SIMVASTATIN 1 0
125930031 12593003 4 C VITAMIN D3 CHOLECALCIFEROL 1 0
125930031 12593003 5 C CALCIUM CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930031 12593003 1 Hypothyroidism
125930031 12593003 3 Product used for unknown indication
125930031 12593003 4 Product used for unknown indication
125930031 12593003 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930031 12593003 Blood thyroid stimulating hormone increased
125930031 12593003 Fatigue

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
125930031 12593003 1 1992 201512 0
125930031 12593003 2 201512 0