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
126940871 12694087 1 I 20160816 20160829 20160829 EXP JP-IMPAX LABORATORIES, INC-2016-IPXL-00922 IMPAX 83.00 YR F Y 0.00000 20160829 MD JP JP

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
126940871 12694087 1 PS MELOXICAM. MELOXICAM 1 Unknown 10 MG, DAILY Y 77930 10 MG TABLET QD
126940871 12694087 2 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown 15 MG, DAILY 0 15 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126940871 12694087 1 Arthralgia
126940871 12694087 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126940871 12694087 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126940871 12694087 Anaemia
126940871 12694087 Chronic gastritis
126940871 12694087 Gastrointestinal disorder
126940871 12694087 Gastrointestinal erosion
126940871 12694087 Gastrointestinal haemorrhage
126940871 12694087 Haematochezia
126940871 12694087 Helicobacter infection
126940871 12694087 Hiatus hernia
126940871 12694087 Intestinal stenosis
126940871 12694087 Large intestinal ulcer
126940871 12694087 Pyrexia
126940871 12694087 Shock

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

no results found

Therapies reported

no results found