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
125930121 12593012 1 I 201601 20160328 20160726 20160726 PER US-ABBVIE-16P-163-1595884-00 ABBVIE 67.63 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
125930121 12593012 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 TABLET
125930121 12593012 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral TAKE WITH ONE TABLET OF 75MCG Y UNKNOWN 21402 TABLET QD
125930121 12593012 3 C CYTOMEL LIOTHYRONINE SODIUM 1 Unknown 0
125930121 12593012 4 C cardio plus 2 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930121 12593012 1 Thyroiditis
125930121 12593012 2 Hypothyroidism
125930121 12593012 3 Product used for unknown indication
125930121 12593012 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930121 12593012 Blood glucose abnormal
125930121 12593012 Blood thyroid stimulating hormone decreased
125930121 12593012 Drug administration error
125930121 12593012 Heart rate increased
125930121 12593012 Hypertension
125930121 12593012 Insomnia
125930121 12593012 Tri-iodothyronine decreased

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
125930121 12593012 1 2002 0
125930121 12593012 2 201601 201601 0
125930121 12593012 3 201602 0