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
127232481 12723248 1 I 20160310 20160322 20160908 20160908 PER US-ZYDUS-010514 ZYDUS PHARM 39.15 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
127232481 12723248 1 PS MELOXICAM. MELOXICAM 1 Oral UNK 77921 15 MG TABLET
127232481 12723248 2 C PREDNISONE. PREDNISONE 1 0
127232481 12723248 3 C CLONAZEPAM. CLONAZEPAM 1 0
127232481 12723248 4 C VITAMINS NOS VITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127232481 12723248 1 Intervertebral disc degeneration
127232481 12723248 2 Product used for unknown indication
127232481 12723248 3 Product used for unknown indication
127232481 12723248 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127232481 12723248 Insomnia Insomnia
127232481 12723248 Oedema Oedema
127232481 12723248 Urticaria 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
127232481 12723248 1 20160310 0