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
124274413 12427441 3 F 20160707 20160602 20160718 EXP US-MLMSERVICE-20160518-0287469-1 US-STRIDES ARCOLAB LIMITED-2016SP004578 STRIDES 0.00 Y 0.00000 20160718 OT GB 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
124274413 12427441 1 PS IBUPROFEN. IBUPROFEN 1 Oral 12 G,TOTAL, 30 PILLS (400 MG) 0 12 G

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124274413 12427441 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124274413 12427441 HO
124274413 12427441 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124274413 12427441 Acute myocardial infarction
124274413 12427441 Cerebrovascular accident
124274413 12427441 Conjunctival pallor
124274413 12427441 Haematuria
124274413 12427441 Intentional overdose
124274413 12427441 Muscular weakness
124274413 12427441 Ocular icterus
124274413 12427441 Sinus tachycardia
124274413 12427441 Suicide attempt
124274413 12427441 Thrombotic thrombocytopenic purpura
124274413 12427441 Unresponsive to stimuli
124274413 12427441 Vitiligo

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

no results found

Therapies reported

no results found