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
113125632 11312563 2 F 20150119 20151016 20150727 20160726 PER US-ABBVIE-15P-163-1337323-00 ABBVIE 69.94 YR F Y 49.03000 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
113125632 11312563 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral TWO (25MCG) TABLETS DAILY 1021519,1019482,1042911 21402 50 UG TABLET BID
113125632 11312563 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown N UNKNOWN 21402
113125632 11312563 3 C CLARITIN-D 12 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 0
113125632 11312563 4 C SINGULAIR MONTELUKAST SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113125632 11312563 1 Hypothyroidism
113125632 11312563 2 Hypothyroidism
113125632 11312563 3 Product used for unknown indication
113125632 11312563 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113125632 11312563 Arthralgia
113125632 11312563 Chills
113125632 11312563 Drug effect decreased
113125632 11312563 Drug ineffective
113125632 11312563 Feeling cold
113125632 11312563 Lethargy
113125632 11312563 Myalgia
113125632 11312563 Pain
113125632 11312563 Product physical issue

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

no results found

Therapies reported

no results found