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
125930771 12593077 1 I 201601 20160303 20160726 20160726 PER US-ABBVIE-16P-163-1575909-00 ABBVIE 41.41 YR F Y 45.40000 KG 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
125930771 12593077 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y 1047533 21402 TABLET
125930771 12593077 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 1/2 TABLET DAILY Y 1047533 21402 TABLET
125930771 12593077 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930771 12593077 1 Thyroidectomy
125930771 12593077 3 Thyroidectomy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930771 12593077 Blood thyroid stimulating hormone decreased
125930771 12593077 Drug effect variable
125930771 12593077 Insomnia
125930771 12593077 Menstruation delayed
125930771 12593077 Palpitations
125930771 12593077 Product quality issue

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
125930771 12593077 1 2013 20160207 0
125930771 12593077 2 20160208 20160209 0
125930771 12593077 3 20160209 0