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
125941321 12594132 1 I 20160711 20160726 20160726 EXP US-AUROBINDO-AUR-APL-2016-09443 AUROBINDO DANG H, ET AL.. IBUPROFEN : ACUTE INTERSTITIAL NEPHRITIS, EVANS SYNDROME AND ACUTE RENAL FAILURE: CASE R. REACTIONS WEEKLY. 2016;1609:67 56.00 YR F Y 0.00000 20160725 OT 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
125941321 12594132 1 PS IBUPROFEN. IBUPROFEN 1 Unknown 3200 MG, DAILY U U 70734 3200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125941321 12594132 1 Headache

Outcome of event

Event ID CASEID OUTC COD
125941321 12594132 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125941321 12594132 Abdominal pain
125941321 12594132 Acute kidney injury
125941321 12594132 Blood lactate dehydrogenase increased
125941321 12594132 Evans syndrome
125941321 12594132 Haemolytic anaemia
125941321 12594132 Headache
125941321 12594132 Nausea
125941321 12594132 Thrombocytopenia
125941321 12594132 Thrombotic thrombocytopenic purpura
125941321 12594132 Tubulointerstitial nephritis
125941321 12594132 Vomiting

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

no results found

Therapies reported

no results found