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
116353392 11635339 2 F 20151115 20151016 20160912 PER US-GLENMARK PHARMACEUTICALS INC, USA.-2015GMK014955 GLENMARK KASHYAP L, ALSAHEEL A, WALVEKAR R, SIMON L, GOMEZ R.. A RARE CASE OF PAINFUL GOITER SECONDARY TO PEDIATRIC HASHIMOTO^S THYROIDITIS REQUIRING THYROIDECTOMY FOR PAIN CONTROL.. PEDIATRIC REPORTS.. 2015;7(3):5914 15.00 YR F Y 72.20000 KG 20160912 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
116353392 11635339 1 PS GABAPENTIN. GABAPENTIN 1 Unknown 300 MG, TID U 77662 300 MG TID
116353392 11635339 2 SS GABAPENTIN. GABAPENTIN 1 Unknown 600 MG, TID U 77662 600 MG TID
116353392 11635339 3 SS IBUPROFEN. IBUPROFEN 1 Unknown 650 MG, BID U 0 650 MG BID
116353392 11635339 4 SS IBUPROFEN. IBUPROFEN 1 Unknown 400 MG, FOUR TIMES DAILY U 0 400 MG
116353392 11635339 5 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 100 ?G, QD U 0 100 UG
116353392 11635339 6 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 112 ?G, QD U 0 112 UG
116353392 11635339 7 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 75 ?G, QD U 0 75 UG
116353392 11635339 8 SS AMITRIPTYLENE AMITRIPTYLINE 1 Unknown 25 MG, OD U 0 25 MG QD
116353392 11635339 9 SS PREDNISONE. PREDNISONE 1 Unknown 2 MG/KG, QD U 0 2 MG/KG
116353392 11635339 10 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown 500 MG, BID U 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116353392 11635339 1 Pain management
116353392 11635339 3 Pain management
116353392 11635339 5 Pain management
116353392 11635339 8 Pain management
116353392 11635339 9 Pain management
116353392 11635339 10 Pain management

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116353392 11635339 Drug ineffective for unapproved indication
116353392 11635339 Rash

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

no results found

Therapies reported

no results found