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
125970171 12597017 1 I 20151026 20160727 20160727 PER US-SUN PHARMACEUTICAL INDUSTRIES LTD-2015US-108286 RANBAXY 0.00 F Y 0.00000 20160727 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
125970171 12597017 1 PS TRAMADOL. TRAMADOL 1 Unknown UNK UNK, DAILY U U 76100
125970171 12597017 2 SS MELOXICAM. MELOXICAM 1 Unknown UNK UNK, DAILY U 0
125970171 12597017 3 SS FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Unknown UNK, DAILY U 0
125970171 12597017 4 SS LYRICA PREGABALIN 1 Unknown 300 MG U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125970171 12597017 1 Fibromyalgia
125970171 12597017 2 Fibromyalgia
125970171 12597017 3 Fibromyalgia
125970171 12597017 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125970171 12597017 Drug ineffective
125970171 12597017 Weight increased

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

no results found

Therapies reported

no results found