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
125931451 12593145 1 I 201604 20160506 20160726 20160726 PER US-ABBVIE-16P-163-1628370-00 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
125931451 12593145 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral ALTERNATES BETWEEN THE 100 MCG AND 112 MCG DAILY. THE 100 MCG 3 TIMES A WEEK 1042490 21402 TABLET TIW
125931451 12593145 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral ALTERNATES BETWEEN THE 100 MCG AND 112 MCG DAILY. THE 112 MCG 4 TIMES A WEEK 1054798,1054798 21402

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125931451 12593145 1 Hypothyroidism
125931451 12593145 2 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125931451 12593145 Ear discomfort
125931451 12593145 Eye pruritus
125931451 12593145 Food allergy
125931451 12593145 Hypersensitivity
125931451 12593145 Oral discomfort
125931451 12593145 Oropharyngeal pain
125931451 12593145 Pruritus
125931451 12593145 Pruritus generalised
125931451 12593145 Rash
125931451 12593145 Seasonal allergy
125931451 12593145 Skin burning sensation
125931451 12593145 Throat irritation
125931451 12593145 Tongue discomfort

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
125931451 12593145 1 201512 0
125931451 12593145 2 201512 0