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
127232351 12723235 1 I 20160203 20160209 20160908 20160908 PER US-ZYDUS-010359 ZYDUS PHARM 56.00 YR F Y 0.00000 20160908 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
127232351 12723235 1 PS MELOXICAM. MELOXICAM 1 Oral UNKNOWN 77921 15 MG TABLET
127232351 12723235 2 C METOPROLOL. METOPROLOL 1 U 0
127232351 12723235 3 C LISINOPRIL. LISINOPRIL 1 U 0
127232351 12723235 4 C MONTELUKAST MONTELUKAST SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127232351 12723235 1 Arthritis
127232351 12723235 2 Hypertension
127232351 12723235 3 Hypertension
127232351 12723235 4 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127232351 12723235 Drug ineffective Drug ineffective
127232351 12723235 Joint stiffness Joint stiffness
127232351 12723235 Joint swelling Joint swelling

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
127232351 12723235 1 20160201 0