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
126173361 12617336 1 I 20150812 20160803 20160803 PER US-ALARA PHARMACEUTICAL CORPORATION-1055800 ALARA 73.00 YR F Y 118.18000 KG 20160803 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
126173361 12617336 1 PS LEVO-T LEVOTHYROXINE SODIUM 1 21342 75 UG
126173361 12617336 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 0 50 MG QD
126173361 12617336 3 SS PROTONIX PANTOPRAZOLE SODIUM 1 68645/492/70 0 40 MG QD
126173361 12617336 4 SS ALLOPURINOL. ALLOPURINOL 1 0 300 MG
126173361 12617336 5 SS VALSARTAN. VALSARTAN 1 0 320 MG
126173361 12617336 6 C TYLENOL ACETAMINOPHEN 1 0
126173361 12617336 7 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
126173361 12617336 8 C Melatonin MELATONIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126173361 12617336 1 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126173361 12617336 Abdominal discomfort
126173361 12617336 Abdominal pain
126173361 12617336 Nausea
126173361 12617336 Nightmare
126173361 12617336 Sleep disorder

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

no results found

Therapies reported

no results found