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
113131162 11313116 2 F 201511 20160711 20150727 20160718 EXP US-ABBVIE-15P-163-1393775-00 ABBVIE 77.04 YR F Y 0.00000 20160718 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
113131162 11313116 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 15N09 21402 75 UG
113131162 11313116 2 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 0 75 MG
113131162 11313116 3 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 0 88 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113131162 11313116 1 Autoimmune thyroiditis
113131162 11313116 2 Autoimmune thyroiditis

Outcome of event

Event ID CASEID OUTC COD
113131162 11313116 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
113131162 11313116 Alopecia
113131162 11313116 Asthenia
113131162 11313116 Blood thyroid stimulating hormone abnormal
113131162 11313116 Blood thyroid stimulating hormone increased
113131162 11313116 Chills
113131162 11313116 Drug effect decreased
113131162 11313116 Drug ineffective
113131162 11313116 Fatigue
113131162 11313116 Nail discolouration
113131162 11313116 Skin discolouration
113131162 11313116 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
113131162 11313116 1 1980 2014 0
113131162 11313116 2 2015 201601 0
113131162 11313116 3 201601 0