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
125285771 12528577 1 I 2016 20160620 20160705 20160705 EXP CA-HQ SPECIALTY-CA-2016INT000451 INTERCHEM 35.00 YR F Y 0.00000 20160705 CN CA CA

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
125285771 12528577 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 2.4286 MG (17 MG, 1 IN 1 W) 201749 17 MG
125285771 12528577 2 C FOLIC ACID. FOLIC ACID 1 UNK U 0
125285771 12528577 3 C IRON IRON 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125285771 12528577 1 Rheumatoid arthritis
125285771 12528577 2 Product used for unknown indication
125285771 12528577 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125285771 12528577 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125285771 12528577 Depression
125285771 12528577 Headache
125285771 12528577 Nasopharyngitis
125285771 12528577 Poor quality sleep
125285771 12528577 Restless legs syndrome
125285771 12528577 Rheumatoid arthritis
125285771 12528577 Tuberculosis

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

no results found

Therapies reported

no results found