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
124414872 12441487 2 F 2015 20160705 20160607 20160707 EXP US-PFIZER INC-2016271282 PFIZER 63.00 YR F Y 0.00000 20160707 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
124414872 12441487 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, DAILY Y 20699 75 MG PROLONGED-RELEASE CAPSULE
124414872 12441487 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, ALTERNATE DAY (2-3 WKS) Y 20699 75 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 3 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 37.5 MG, ALTERNATE DAY (3 WKS) Y 20699 37.5 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 4 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 30 MG, ALTERNATE DAY (1 WK) Y 20699 30 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 5 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 25 MG, ALTERNATE DAY (1 WK) Y 20699 25 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 6 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 20 MG, ALTERNATE DAY (3 WKS) Y 20699 20 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 7 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 15 MG, ALTERNATE DAY (2 DOSES) Y 20699 15 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 8 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 10 MG, ALTERNATE DAY (3 DOSES) Y 20699 10 MG PROLONGED-RELEASE CAPSULE QOD
124414872 12441487 9 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 5 MG, UNK (2 DOSES) Y 20699 5 MG PROLONGED-RELEASE CAPSULE
124414872 12441487 10 C LOPRESSOR METOPROLOL TARTRATE 1 50 MG, 2X/DAY 0 50 MG BID
124414872 12441487 11 C LOPRESSOR METOPROLOL TARTRATE 1 50 MG, DAILY 0 50 MG
124414872 12441487 12 C SYNTHROID LEVOTHYROXINE SODIUM 1 100 UG, DAILY 0 100 UG
124414872 12441487 13 C PROTONIX PANTOPRAZOLE SODIUM 1 40 MG, DAILY 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124414872 12441487 1 Depression
124414872 12441487 2 Anxiety
124414872 12441487 10 Supraventricular tachycardia
124414872 12441487 12 Thyroid disorder
124414872 12441487 13 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
124414872 12441487 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124414872 12441487 Abdominal pain upper
124414872 12441487 Auditory disorder
124414872 12441487 Dizziness
124414872 12441487 Drug intolerance
124414872 12441487 Feeling abnormal
124414872 12441487 Heart rate irregular
124414872 12441487 Memory impairment
124414872 12441487 Nausea
124414872 12441487 Nystagmus
124414872 12441487 Paraesthesia
124414872 12441487 Tinnitus
124414872 12441487 Vomiting
124414872 12441487 Withdrawal syndrome

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
124414872 12441487 1 201307 201603 0
124414872 12441487 2 201603 2016 0
124414872 12441487 3 2016 2016 0
124414872 12441487 4 2016 2016 0
124414872 12441487 5 2016 2016 0
124414872 12441487 6 2016 2016 0
124414872 12441487 7 2016 2016 0
124414872 12441487 8 2016 2016 0
124414872 12441487 9 2016 201605 0
124414872 12441487 10 1981 0