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
113137012 11313701 2 F 2013 20160506 20150727 20160726 PER US-ABBVIE-15P-163-1417952-00 ABBVIE 0.00 F Y 44.00000 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
113137012 11313701 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 TABLET QD
113137012 11313701 2 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral TOOK FOR 20-25 YEARS 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113137012 11313701 1 Hypothyroidism
113137012 11313701 2 Autoimmune thyroiditis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113137012 11313701 Drug ineffective
113137012 11313701 Eye pruritus
113137012 11313701 Feeling abnormal
113137012 11313701 Hypersensitivity
113137012 11313701 Hypertension
113137012 11313701 Nasal congestion
113137012 11313701 Panic attack
113137012 11313701 Photosensitivity reaction
113137012 11313701 Product odour abnormal
113137012 11313701 Product quality issue
113137012 11313701 Vertigo
113137012 11313701 Wheezing

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
113137012 11313701 1 2013 201507 0
113137012 11313701 2 2013 0