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
126578291 12657829 1 I 20160811 20160817 20160817 EXP IT-STRIDES ARCOLAB LIMITED-2016SP011802 STRIDES 0.00 Y 0.00000 20160817 OT 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
126578291 12657829 1 PS IBUPROFEN. IBUPROFEN 1 100 MG, DAILY U U 0 100 MG
126578291 12657829 2 SS Paracetamol ACETAMINOPHEN 1 UNK U U 0
126578291 12657829 3 SS BETAMETHASONE. BETAMETHASONE 1 UNK 0
126578291 12657829 4 C CEFPODOXIME CEFPODOXIME 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126578291 12657829 1 Pyrexia
126578291 12657829 2 Pyrexia
126578291 12657829 3 Product used for unknown indication
126578291 12657829 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126578291 12657829 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126578291 12657829 Bradyarrhythmia
126578291 12657829 Hyperhidrosis
126578291 12657829 Hypothermia
126578291 12657829 Off label use
126578291 12657829 Pallor

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

no results found

Therapies reported

no results found