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
127792671 12779267 1 I 0 20160923 20160923 DIR FDA-CTU 0.00 N 0.00000 0 N 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
127792671 12779267 1 PS IBUPROFEN 600MG TABS IBUPROFEN 1 Oral 13343A 20160820 0 600 MG COATED TABLET HS
127792671 12779267 2 SS CYCLOBENZAPRINE HCL 10 MG TABS CYCLOBENZAPRINE HYDROCHLORIDE 1 HA09616 20160820 0
127792671 12779267 4 C PREDNISONE. PREDNISONE 1 0
127792671 12779267 6 C ALEVE NAPROXEN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127792671 12779267 1 Muscle spasms
127792671 12779267 1 Post-traumatic neck syndrome
127792671 12779267 1 Road traffic accident

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127792671 12779267 Headache
127792671 12779267 Heart rate increased
127792671 12779267 Malaise

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127792671 12779267 1 20160820 20160821 0
127792671 12779267 2 20160820 20160821 0