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
125929421 12592942 1 I 2015 20150811 20160726 20160726 PER US-ABBVIE-15P-163-1448098-00 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
125929421 12592942 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 75 UG TABLET QD
125929421 12592942 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 75 UG TABLET QD
125929421 12592942 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 88 UG TABLET QD
125929421 12592942 4 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN,UNKNOWN,UNKNOWN 21402 100 UG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125929421 12592942 1 Hypothyroidism
125929421 12592942 3 Hypothyroidism
125929421 12592942 4 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125929421 12592942 Blood thyroid stimulating hormone decreased
125929421 12592942 Erythema
125929421 12592942 Insomnia
125929421 12592942 Palpitations
125929421 12592942 Rash
125929421 12592942 Skin burning sensation
125929421 12592942 Sluggishness

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
125929421 12592942 1 1996 0
125929421 12592942 2 201506 0
125929421 12592942 3 2015 2015 0
125929421 12592942 4 2015 201506 0