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
108135443 10813544 3 F 201310 20160722 20150218 20160726 EXP US-PFIZER INC-2015058792 PFIZER 64.00 YR F Y 89.00000 KG 20160726 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
108135443 10813544 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, DAILY 21992 50 MG PROLONGED-RELEASE TABLET
108135443 10813544 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 100 MG, 1X/DAY 21992 100 MG PROLONGED-RELEASE TABLET
108135443 10813544 3 C VALPROIC ACID. VALPROIC ACID 1 Oral 250 MG, AS NEEDED 0 250 MG TABLET
108135443 10813544 4 C BACLOFEN. BACLOFEN 1 20 MG, 3X/DAY C080 10 15A 0 20 MG TABLET TID
108135443 10813544 5 C BACLOFEN. BACLOFEN 1 Oral 10 MG, ONCE AT NIGHT 0 10 MG TABLET
108135443 10813544 6 C DIAZEPAM. DIAZEPAM 1 Oral 5 MG, 2X/DAY 106028A 0 5 MG TABLET BID
108135443 10813544 7 C MAGNESIUM MAGNESIUM 1 Oral 800 MG, DAILY 0 800 MG TABLET
108135443 10813544 8 C SUMATRIPTAN SUCCINATE. SUMATRIPTAN SUCCINATE 1 50 MG, AS NEEDED (ONE OR TWO TABLETS AS NEEDED) 0 50 MG TABLET
108135443 10813544 9 C METHYLPHENIDATE. METHYLPHENIDATE 1 10 MG, 1X/DAY 0 10 MG TABLET QD
108135443 10813544 10 C METHYLPHENIDATE. METHYLPHENIDATE 1 0 TABLET
108135443 10813544 11 C METHYLPHENIDATE. METHYLPHENIDATE 1 0 TABLET
108135443 10813544 12 C CLARITIN LORATADINE 1 10 MG, ONE EVERY TWO WEEKS 0 10 MG TABLET
108135443 10813544 13 C CLARITIN LORATADINE 1 0 TABLET
108135443 10813544 14 C BUPROPION HCL BUPROPION HYDROCHLORIDE 1 100 MG, 1X/DAY 0 100 MG MODIFIED-RELEASE TABLET QD
108135443 10813544 15 C BUPROPION HCL BUPROPION HYDROCHLORIDE 1 0 MODIFIED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108135443 10813544 1 Major depression
108135443 10813544 2 Crying
108135443 10813544 3 Headache
108135443 10813544 4 Muscle spasms
108135443 10813544 5 Pain
108135443 10813544 8 Migraine
108135443 10813544 9 Attention deficit/hyperactivity disorder
108135443 10813544 10 Fatigue
108135443 10813544 11 Somnolence
108135443 10813544 12 Hypersensitivity
108135443 10813544 13 Asthma
108135443 10813544 14 Asthenia
108135443 10813544 15 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
108135443 10813544 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108135443 10813544 Arthralgia
108135443 10813544 Migraine
108135443 10813544 Muscle spasms
108135443 10813544 Pain in extremity
108135443 10813544 Paraesthesia
108135443 10813544 Suicide attempt

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
108135443 10813544 2 201001 0
108135443 10813544 4 2014 0
108135443 10813544 5 201411 0
108135443 10813544 6 2011 0
108135443 10813544 8 201409 0
108135443 10813544 9 201406 0
108135443 10813544 12 2008 0
108135443 10813544 14 2009 0