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
127252031 12725203 1 I 20160820 0 20160905 20160905 DIR US-FDA-349802 FDA-CTU 62.00 YR M N 81.00000 KG 20160905 N 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
127252031 12725203 1 PS ISONIAZID. ISONIAZID 1 Oral Y Y 0 QD
127252031 12725203 2 C PREDNISONE. PREDNISONE 1 0
127252031 12725203 3 C MESALAMINE. MESALAMINE 1 0
127252031 12725203 4 C MULTI VITAMIN VITAMINS 1 0
127252031 12725203 5 C B-6 2 0
127252031 12725203 6 C POTASSIUM POTASSIUM 1 0
127252031 12725203 7 C MAGNESIUM MAGNESIUM 1 0
127252031 12725203 8 C VITAMIN D CHOLECALCIFEROL 1 0
127252031 12725203 9 C FISH OIL FISH OIL 1 0
127252031 12725203 10 C WOBENSYM 2 0
127252031 12725203 11 C TUMERIC TURMERIC 1 0
127252031 12725203 12 C SCHIFF MOVE FREE CHONDROITIN SULFATE AGLUCOSAMINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127252031 12725203 1 Latent tuberculosis

Outcome of event

Event ID CASEID OUTC COD
127252031 12725203 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127252031 12725203 Bone pain
127252031 12725203 Confusional state
127252031 12725203 Drug-induced liver injury
127252031 12725203 Fatigue
127252031 12725203 Hyperhidrosis
127252031 12725203 Malaise
127252031 12725203 Myalgia
127252031 12725203 Nausea
127252031 12725203 Pyrexia
127252031 12725203 Tremor
127252031 12725203 Vomiting

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
127252031 12725203 1 20160801 20160821 0