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
125720441 12572044 1 I 20160706 20160719 20160719 EXP JP-BAUSCH-BL-2016-016871 BAUSCH AND LOMB FUJII K, MIYASHITA K, KURIHARA I, HIRATSUKA K, SATO S, YOKOTA K. ADRENAL INSUFFICIENCY UNDER STANDARD DOSAGE OF GLUCOCORTICOID REPLACEMENT AFTER UNILATERAL ADRENALECTOMY FOR CUSHING^S SYNDROME. CASE REPORTS IN ENDOCRINOLOGY. 2016;. 62.00 YR F Y 0.00000 20160719 MD JP JP

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
125720441 12572044 1 PS HYDROCORTISONE. HYDROCORTISONE 1 Oral Y 18514 200 MG
125720441 12572044 2 SS HYDROCORTISONE. HYDROCORTISONE 1 Oral Y 18514 30 MG
125720441 12572044 3 C CIBENZOLINE CIFENLINE 1 0
125720441 12572044 4 C DEXAMETHASONE. DEXAMETHASONE 1 0 8 MG
125720441 12572044 5 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0
125720441 12572044 6 C BISOPROLOL BISOPROLOL 1 0
125720441 12572044 7 C FUROSEMIDE. FUROSEMIDE 1 0
125720441 12572044 8 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
125720441 12572044 9 C ENTECAVIR. ENTECAVIR 1 0
125720441 12572044 10 C LOVASTATIN. LOVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125720441 12572044 1 Cushing's syndrome
125720441 12572044 3 Product used for unknown indication
125720441 12572044 4 Product used for unknown indication
125720441 12572044 5 Product used for unknown indication
125720441 12572044 6 Product used for unknown indication
125720441 12572044 7 Fluid retention
125720441 12572044 8 Product used for unknown indication
125720441 12572044 9 Product used for unknown indication
125720441 12572044 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125720441 12572044 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125720441 12572044 Decreased appetite
125720441 12572044 Fatigue
125720441 12572044 Malabsorption
125720441 12572044 Nausea

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

no results found

Therapies reported

no results found