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
106442432 10644243 2 F 2014 20160725 20141210 20160728 EXP US-PFIZER INC-2014329559 PFIZER 53.00 YR F Y 92.97000 KG 20160728 CN 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
106442432 10644243 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 225 MG, 3X/DAY 20699 225 MG PROLONGED-RELEASE CAPSULE TID
106442432 10644243 2 C LEVOTHYROXINE. LEVOTHYROXINE 1 Oral 0.112 MG, 1X/DAY 0 .112 MG QD
106442432 10644243 3 C CALCIUM + VIT D CALCIUMVITAMIN D 1 Oral UNK, 2X/DAY (600/400) 0 TABLET BID
106442432 10644243 4 C LEVETIRACETAM. LEVETIRACETAM 1 Oral 500 MG, UNK (500MG TABLET ONE IN THE MORNING AND 2 AT NIGHT) 0 500 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106442432 10644243 1 Depression
106442432 10644243 2 Thyroid disorder
106442432 10644243 4 Seizure

Outcome of event

Event ID CASEID OUTC COD
106442432 10644243 HO
106442432 10644243 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106442432 10644243 Arthralgia
106442432 10644243 Autoimmune thyroiditis
106442432 10644243 Haematemesis
106442432 10644243 Hypertension
106442432 10644243 Malaise
106442432 10644243 Migraine
106442432 10644243 Portal venous gas
106442432 10644243 Vomiting

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

no results found

Therapies reported

no results found