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
105659803 10565980 3 F 20160804 20141105 20160808 PER US-PFIZER INC-2014304054 PFIZER 48.00 YR F Y 58.96000 KG 20160808 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
105659803 10565980 1 PS LYRICA PREGABALIN 1 Oral 100 MG, 3X/DAY U 21446 100 MG CAPSULE, HARD TID
105659803 10565980 2 SS LYRICA PREGABALIN 1 U 21446 CAPSULE, HARD
105659803 10565980 3 C ELAVIL AMITRIPTYLINE HYDROCHLORIDE 1 50 MG, UNK 0 50 MG
105659803 10565980 4 C OXYCODONE OXYCODONE 1 5 MG, UNK 0 5 MG
105659803 10565980 5 C LORAZEPAM. LORAZEPAM 1 0.5 MG, UNK 0 .5 MG
105659803 10565980 6 C PROPRANOLOL ER 2 120 MG, UNK 0 120 MG
105659803 10565980 7 C TOPAMAX TOPIRAMATE 1 50 MG, UNK 0 50 MG
105659803 10565980 8 C SUMATRIPTAN. SUMATRIPTAN 1 100 MG, AS NEEDED 0 100 MG
105659803 10565980 9 C OMEPRAZOLE. OMEPRAZOLE 1 40 MG, UNK 0 40 MG
105659803 10565980 10 C MISOPROSTOL. MISOPROSTOL 1 100 UG, UNK 0 100 UG
105659803 10565980 11 C CARAFATE SUCRALFATE 1 UNK 0
105659803 10565980 12 C BACLOFEN. BACLOFEN 1 10 MG, 1X/DAY(AT NIGHT) 0 10 MG QD
105659803 10565980 13 C BACLOFEN. BACLOFEN 1 0.5 MG, UNK 0 .5 MG
105659803 10565980 14 C BACLOFEN. BACLOFEN 1 0
105659803 10565980 15 C BACLOFEN. BACLOFEN 1 0
105659803 10565980 16 C MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 10 MG, UNK 0 10 MG
105659803 10565980 17 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 100 MG, UNK 0 100 MG
105659803 10565980 18 C MUPIROCIN. MUPIROCIN 1 UNK 0 OINTMENT
105659803 10565980 19 C AMITRIPTYLINE AMITRIPTYLINE 1 100 MG, UNK 0 100 MG
105659803 10565980 20 C MIDODRINE MIDODRINE 1 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105659803 10565980 1 Pain
105659803 10565980 2 Cancer pain
105659803 10565980 3 Cancer pain
105659803 10565980 4 Cancer pain
105659803 10565980 5 Cancer pain
105659803 10565980 6 Migraine
105659803 10565980 7 Migraine
105659803 10565980 8 Migraine
105659803 10565980 9 Gastrooesophageal reflux disease
105659803 10565980 10 Gastrooesophageal reflux disease
105659803 10565980 11 Gastrooesophageal reflux disease
105659803 10565980 12 Gastrooesophageal reflux disease
105659803 10565980 13 Dyspepsia
105659803 10565980 14 Chest pain
105659803 10565980 15 Breast pain
105659803 10565980 16 Asthma
105659803 10565980 17 Depression
105659803 10565980 18 Nasal dryness
105659803 10565980 19 Breast pain
105659803 10565980 20 Hypotension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
105659803 10565980 Dry mouth
105659803 10565980 Product use issue

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

no results found

Therapies reported

no results found