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
123891362 12389136 2 F 2014 20160727 20160520 20160803 EXP BR-ABBVIE-16P-020-1633465-00 ABBVIE 0.00 F Y 64.00000 KG 20160803 CN COUNTRY NOT SPECIFIED BR

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
123891362 12389136 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNKNOWN 21402 50 UG QD
123891362 12389136 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown DAILY DOSE: 175 MCG (2 TABLETS OF 50MCG AND 1 TABLET OF 75MCG) UNKNOWN 21402
123891362 12389136 3 C ALLEGRA-D FEXOFENADINEPSEUDOEPHEDRINE 1 POSOLOGY UNKNOWN (PATIENT IS NOT TAKING THE PRODUCT NOWADAYS) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123891362 12389136 1 Thyroid disorder
123891362 12389136 3 Hypersensitivity

Outcome of event

Event ID CASEID OUTC COD
123891362 12389136 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123891362 12389136 Blood thyroid stimulating hormone increased
123891362 12389136 Papillary thyroid cancer

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
123891362 12389136 1 2011 2014 0
123891362 12389136 2 2014 0