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
125931211 12593121 1 I 2013 20160328 20160726 20160726 PER US-ABBVIE-16P-163-1593474-00 ABBVIE 0.00 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
125931211 12593121 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y 21402 TABLET QD
125931211 12593121 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN,UNKNOWN 21402 TABLET QD
125931211 12593121 3 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125931211 12593121 1 Hypothyroidism
125931211 12593121 2 Hypothyroidism
125931211 12593121 3 Vitamin D deficiency

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125931211 12593121 Anxiety
125931211 12593121 Blood thyroid stimulating hormone increased
125931211 12593121 Chest discomfort
125931211 12593121 Malabsorption
125931211 12593121 Palpitations

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
125931211 12593121 1 2013 2013 0
125931211 12593121 2 2013 0