The Safety Rates Drug Report

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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
101459384 10145938 4 F 20130706 20160707 20140501 20160712 EXP PHHY2014PL051655 NOVARTIS KACZMARSKA-TUREK D, BARTNIK PJ, ORLEWSKI J. TOXIC EPIDERMAL NECROLYSIS IN PATIENT WITH MALIGNANT ASTROCYTOMA. 287 (88) 62.00 YR M Y 0.00000 20160713 OT PL PL

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
101459384 10145938 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 400 MG, BID Y 16608 400 MG TABLET BID
101459384 10145938 2 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 2 MG, TID U 0 2 MG TID
101459384 10145938 3 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, QID U 0 40 MG QID
101459384 10145938 4 C DIGOXIN. DIGOXIN 1 Oral 0.125 MG, QID U 0 .125 MG QID
101459384 10145938 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 25 MG, QID U 0 25 MG QID
101459384 10145938 6 C FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, QID U 0 40 MG QID
101459384 10145938 7 C CLEMASTINUM CLEMASTINE FUMARATE 1 Oral 1 MG, QID U 0 1 MG QID
101459384 10145938 8 C ENOXAPARIN ENOXAPARIN 1 Subcutaneous 100 MG, QID U 0 100 MG QID
101459384 10145938 9 C METOPROLOL. METOPROLOL 1 Oral 25 MG, TID U 0 25 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101459384 10145938 1 Epilepsy
101459384 10145938 2 Product used for unknown indication
101459384 10145938 3 Product used for unknown indication
101459384 10145938 4 Product used for unknown indication
101459384 10145938 5 Product used for unknown indication
101459384 10145938 6 Product used for unknown indication
101459384 10145938 7 Product used for unknown indication
101459384 10145938 8 Product used for unknown indication
101459384 10145938 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101459384 10145938 HO
101459384 10145938 OT
101459384 10145938 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101459384 10145938 Blister
101459384 10145938 Conjunctivitis
101459384 10145938 Dehydration
101459384 10145938 Drug interaction
101459384 10145938 Erythema
101459384 10145938 Hyperaemia
101459384 10145938 Mucosal haemorrhage
101459384 10145938 Pyrexia
101459384 10145938 Scab
101459384 10145938 Staphylococcal sepsis
101459384 10145938 Toxic epidermal necrolysis

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
101459384 10145938 1 201305 201307 0