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
127388371 12738837 1 I 20160829 20160912 20160912 EXP AU-IPCA LABORATORIES LIMITED-IPC201609-000739 IPCA BOYD I. THIAMAZOLE AND RHABDOMYOLYSIS. WHO PHARMACEUTICALS NEWSLETTER 2016 AUG 17;4:17-23. 33.00 YR M Y 0.00000 20160912 OT AU AU

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
127388371 12738837 1 PS FUROSEMIDE. FUROSEMIDE 1 U 78010
127388371 12738837 2 SS Warfarin WARFARIN 1 U 200104
127388371 12738837 3 SS ALPRAZOLAM. ALPRAZOLAM 1 U 0
127388371 12738837 4 SS Bisoprolol BISOPROLOL 1 U 0
127388371 12738837 5 SS Candesartan CANDESARTAN 1 U 0
127388371 12738837 6 SS LANSOPRAZOLE. LANSOPRAZOLE 1 U 0
127388371 12738837 7 SS PROPYLTHIOURACIL. PROPYLTHIOURACIL 1 U 0
127388371 12738837 8 SS SPIRONOLACTONE. SPIRONOLACTONE 1 U 0
127388371 12738837 9 SS Thiamazole METHIMAZOLE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127388371 12738837 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127388371 12738837 Rhabdomyolysis

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

no results found

Therapies reported

no results found