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
127172593 12717259 3 F 20160831 20160906 20160906 EXP PHHY2016AR121952 SANDOZ 0.00 E F Y 0.00000 20160906 CN AR AR

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
127172593 12717259 1 PS DICLOFENAC DICLOFENAC 1 Unknown U 74376
127172593 12717259 2 C ALPLAX 2 Unknown 1 MG, UNK U 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127172593 12717259 1 Product used for unknown indication
127172593 12717259 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127172593 12717259 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127172593 12717259 Arterial disorder
127172593 12717259 Blood pressure increased
127172593 12717259 Dyspepsia
127172593 12717259 Exostosis
127172593 12717259 Musculoskeletal discomfort
127172593 12717259 Neck pain
127172593 12717259 Nervousness
127172593 12717259 Night blindness
127172593 12717259 Osteoarthritis
127172593 12717259 Pain
127172593 12717259 Retinal vascular thrombosis
127172593 12717259 Spinal disorder
127172593 12717259 Visual impairment

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

no results found

Therapies reported

no results found