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
123860305 12386030 5 F 201509 20160720 20160519 20160901 EXP BR-ABBVIE-16P-020-1632228-00 ABBVIE 56.26 YR F Y 67.00000 KG 20160901 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
123860305 12386030 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402
123860305 12386030 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral DAILY DOSE: 50 MCG; ONCE A DAY, IN THE MORNING UNKNOWN 21402 50 UG QD
123860305 12386030 3 C GLAUB BRIMONIDINE TARTRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123860305 12386030 1 Hypothyroidism
123860305 12386030 3 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
123860305 12386030 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123860305 12386030 Alopecia
123860305 12386030 Blood thyroid stimulating hormone increased
123860305 12386030 Dry skin
123860305 12386030 Glaucoma
123860305 12386030 Hair texture abnormal

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
123860305 12386030 1 2001 2004 0
123860305 12386030 2 2012 0