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
125932241 12593224 1 I 201512 20160525 20160726 20160726 PER US-ABBVIE-16P-163-1637743-00 ABBVIE 60.42 YR F Y 77.18000 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
125932241 12593224 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral U UNKNOWN 21402 125 UG QD
125932241 12593224 2 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 0 137 UG QD
125932241 12593224 3 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 0 137 UG QD
125932241 12593224 4 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Oral N 0 200 UG QD
125932241 12593224 5 C THYROXINE LEVOTHYROXINE 1 Oral 0 125 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125932241 12593224 1 Product used for unknown indication
125932241 12593224 2 Thyroidectomy
125932241 12593224 4 Thyroidectomy
125932241 12593224 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125932241 12593224 Bone pain
125932241 12593224 Drug ineffective
125932241 12593224 Irritability
125932241 12593224 Palpitations
125932241 12593224 Renal impairment
125932241 12593224 Skin discolouration

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
125932241 12593224 1 2008 0
125932241 12593224 2 2000 2013 0
125932241 12593224 3 2013 0
125932241 12593224 4 2007 0