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
126906631 12690663 1 I 20160627 20160816 20160826 20160826 EXP IT-MINISAL02-371343 IT-TEVA-686543ACC TEVA 55.68 YR F Y 0.00000 20160826 MD IT IT

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
126906631 12690663 1 PS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral 20 DOSAGE FORMS DAILY; Y 75977 20 DF ORAL DROPS
126906631 12690663 2 C TACHIDOL ACETAMINOPHENCODEINE PHOSPHATE 1 Oral U 0
126906631 12690663 3 C TORA-DOL KETOROLAC TROMETHAMINE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126906631 12690663 1 Back pain
126906631 12690663 2 Product used for unknown indication
126906631 12690663 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126906631 12690663 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126906631 12690663 Adverse drug reaction
126906631 12690663 Asthenia
126906631 12690663 Feeling abnormal
126906631 12690663 Hyperhidrosis
126906631 12690663 Palpitations

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
126906631 12690663 1 20160627 20160627 0