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
125930581 12593058 1 I 20160523 20160726 20160726 PER US-ABBVIE-16P-163-1639310-00 ABBVIE 53.00 YR M Y 83.99000 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
125930581 12593058 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral U UNKNOWN 21402 137 UG TABLET QD
125930581 12593058 2 SS ARMOUR THYROID THYROID, PORCINE 1 Unknown Y UNKNOWN 0 200 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930581 12593058 1 Hypothyroidism
125930581 12593058 2 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930581 12593058 Anxiety
125930581 12593058 Blood thyroid stimulating hormone decreased
125930581 12593058 Hyperthyroidism
125930581 12593058 Insomnia
125930581 12593058 Nervousness
125930581 12593058 Panic attack
125930581 12593058 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found