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
125930821 12593082 1 I 201603 20160408 20160726 20160726 PER US-ABBVIE-16P-163-1602415-00 ABBVIE 71.29 YR M Y 0.00000 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
125930821 12593082 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 TABLET QD
125930821 12593082 2 C WARFARIN WARFARIN 1 0
125930821 12593082 3 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 0
125930821 12593082 4 C CEPHALEXIN. CEPHALEXIN 1 0
125930821 12593082 5 C PREDNISONE. PREDNISONE 1 0
125930821 12593082 6 C FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930821 12593082 1 Hypothyroidism
125930821 12593082 2 Product used for unknown indication
125930821 12593082 3 Product used for unknown indication
125930821 12593082 4 Product used for unknown indication
125930821 12593082 5 Product used for unknown indication
125930821 12593082 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930821 12593082 Fatigue
125930821 12593082 Muscle spasms
125930821 12593082 Product quality issue

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

no results found

Therapies reported

no results found