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
106897167 10689716 7 F 20150529 20160923 20150105 20160928 EXP US-PFIZER INC-2014363628 PFIZER 50.00 YR F Y 0.00000 20160928 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
106897167 10689716 1 PS LYRICA PREGABALIN 1 Oral 100 MG, 3X/DAY 21446 100 MG CAPSULE, HARD TID
106897167 10689716 2 SS LYRICA PREGABALIN 1 Oral 100 MG, UNK 21446 100 MG CAPSULE, HARD
106897167 10689716 3 SS LYRICA PREGABALIN 1 Oral 300 MG, DAILY 21446 300 MG CAPSULE, HARD
106897167 10689716 4 C LORAZEPAM. LORAZEPAM 1 UNK 0
106897167 10689716 5 C DICYCLOMINE DICYCLOMINE HYDROCHLORIDE 1 UNK 0
106897167 10689716 6 C ALBUTEROL. ALBUTEROL 1 UNK 0
106897167 10689716 7 C PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 UNK 0
106897167 10689716 8 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0
106897167 10689716 9 C REMERON MIRTAZAPINE 1 UNK 0
106897167 10689716 10 C ADVIL IBUPROFEN 1 UNK 0
106897167 10689716 11 C LEVOTHYROXIN LEVOTHYROXINE 1 UNK 0
106897167 10689716 12 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UNK 0
106897167 10689716 13 C VITAMIN D2 ERGOCALCIFEROL 1 UNK 0
106897167 10689716 14 C MORPHINE MORPHINE 1 Oral 150 MG, 3X/DAY 0 150 MG TABLET TID
106897167 10689716 15 C MORPHINE MORPHINE 1 Oral 30 MG, EVERY 8 HOURS 0 30 MG PROLONGED-RELEASE TABLET TID
106897167 10689716 16 C MORPHINE MORPHINE 1 Oral 15 MG, 4X/DAY 0 15 MG TABLET QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106897167 10689716 1 Fibromyalgia
106897167 10689716 2 Neuropathy peripheral

Outcome of event

Event ID CASEID OUTC COD
106897167 10689716 OT
106897167 10689716 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106897167 10689716 Abasia
106897167 10689716 Anger
106897167 10689716 Anxiety
106897167 10689716 Arrhythmia
106897167 10689716 Autoimmune disorder
106897167 10689716 Blood pressure increased
106897167 10689716 Drug dependence
106897167 10689716 Drug ineffective
106897167 10689716 Heart rate increased
106897167 10689716 Hypersensitivity
106897167 10689716 Malaise
106897167 10689716 Nasopharyngitis
106897167 10689716 Oxygen saturation decreased
106897167 10689716 Pain
106897167 10689716 Panic attack
106897167 10689716 Post-traumatic stress disorder
106897167 10689716 Sinusitis
106897167 10689716 Thyroid neoplasm
106897167 10689716 Toxicity to various agents
106897167 10689716 Type 2 diabetes mellitus
106897167 10689716 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
106897167 10689716 1 201505 0
106897167 10689716 2 201505 0
106897167 10689716 16 20141225 0