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
126222051 12622205 1 I 20160727 20160804 20160804 EXP US-MYLANLABS-2016M1031779 MYLAN HYLAND KA, WEBER TJ. UNRECOGNIZED MILK-ALKALI SYNDROME WITH HYPOCALCEMIA FOLLOWING BISPHOSPHONATE TREATMENT. ENDOCR-REV 2014. 0.00 Y 0.00000 20160804 OT US US

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
126222051 12622205 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG (ON HOSPITAL DAY 2) U U 202650 INJECTION
126222051 12622205 2 SS ESOMEPRAZOLE ESOMEPRAZOLE 1 Unknown U U 0
126222051 12622205 3 SS TUMS /00193601/ CALCIUM CARBONATEMAGNESIUM CARBONATEMAGNESIUM TRISILICATE 1 Unknown UP TO 6 TIMES PER DAY U U 0
126222051 12622205 4 C TACROLIMUS. TACROLIMUS 1 Unknown 0
126222051 12622205 5 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown 0
126222051 12622205 6 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown 0
126222051 12622205 7 C GANCICLOVIR. GANCICLOVIR 1 Unknown 0
126222051 12622205 8 C FUROSEMIDE. FUROSEMIDE 1 Intravenous (not otherwise specified) 0
126222051 12622205 9 C CALCITONIN CALCITONIN 1 Subcutaneous 200 MICROG EVERY 6 HOURS 0
126222051 12622205 10 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 Unknown DAILY SUPPLEMENT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126222051 12622205 1 Hypercalcaemia
126222051 12622205 2 Gastrooesophageal reflux disease
126222051 12622205 3 Product used for unknown indication
126222051 12622205 4 Product used for unknown indication
126222051 12622205 5 Product used for unknown indication
126222051 12622205 6 Product used for unknown indication
126222051 12622205 7 Product used for unknown indication
126222051 12622205 8 Hypercalcaemia
126222051 12622205 9 Hypercalcaemia

Outcome of event

Event ID CASEID OUTC COD
126222051 12622205 HO
126222051 12622205 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126222051 12622205 Hypocalcaemia
126222051 12622205 Milk-alkali syndrome

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

no results found

Therapies reported

no results found