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
127708161 12770816 1 I 20160808 0 20160922 20160922 DIR FDA-CTU 67.00 YR M N 240.00000 LBS 20160913 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
127708161 12770816 1 PS MELOXICAM. MELOXICAM 1 Oral 1 TABLET DAILY ONCE MOUTH Y D 0 15 MG COATED TABLET QD
127708161 12770816 2 C MELATONIN MELATONIN 1 0
127708161 12770816 3 C BAYER ASPIRIN ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127708161 12770816 1 Arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127708161 12770816 Chest discomfort
127708161 12770816 Dysphonia
127708161 12770816 Lip swelling
127708161 12770816 Pruritus
127708161 12770816 Rash
127708161 12770816 Speech disorder
127708161 12770816 Swollen tongue
127708161 12770816 Throat tightness
127708161 12770816 Urticaria

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
127708161 12770816 1 20160808 20160814 0