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
126589861 12658986 1 I 20151021 20160816 20160816 PER US-APOTEX-2015AP013883 APOTEX 0.00 F Y 0.00000 20160816 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
126589861 12658986 1 PS MELOXICAM. MELOXICAM 1 Unknown UNK UNK, UNKNOWN U 77882 TABLET
126589861 12658986 2 SS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN U 0 TABLET
126589861 12658986 3 SS FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126589861 12658986 1 Fibromyalgia
126589861 12658986 2 Fibromyalgia
126589861 12658986 3 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126589861 12658986 Drug effect incomplete
126589861 12658986 Off label use

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

no results found

Therapies reported

no results found