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
106956158 10695615 8 F 201506 20160926 20150107 20160930 EXP US-PFIZER INC-2015004178 PFIZER 76.00 YR F Y 44.90000 KG 20160930 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
106956158 10695615 1 PS LYRICA PREGABALIN 1 Oral 25 MG, UNK N 21446 25 MG CAPSULE, HARD
106956158 10695615 2 SS LYRICA PREGABALIN 1 Oral 300 MG, 3X/DAY N 21446 300 MG CAPSULE, HARD TID
106956158 10695615 3 SS LYRICA PREGABALIN 1 Oral 300 MG, 3X/DAY N M22778 21446 300 MG CAPSULE, HARD TID
106956158 10695615 4 SS LYRICA PREGABALIN 1 UNK, 2X/DAY N 21446 CAPSULE, HARD BID
106956158 10695615 5 C LASIX FUROSEMIDE 1 UNK 0
106956158 10695615 6 C FUROSEMIDE. FUROSEMIDE 1 UNK 0
106956158 10695615 7 C DIAZEPAM. DIAZEPAM 1 10 MG, DAILY 0 10 MG
106956158 10695615 8 C AMBIEN ZOLPIDEM TARTRATE 1 UNK 0
106956158 10695615 9 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, 2X/DAY 0 20 MG CAPSULE BID
106956158 10695615 10 C DIGOXIN. DIGOXIN 1 Oral 125 UG, 1X/DAY 0 125 UG TABLET QD
106956158 10695615 11 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 UNK 0
106956158 10695615 12 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0
106956158 10695615 13 C TRIAMTERENE. TRIAMTERENE 1 Oral 37.5-25MG CT ONE CAPSULE 0 1 DF CAPSULE
106956158 10695615 14 C HYDROXYZINE HCL HYDROXYZINE HYDROCHLORIDE 1 Oral 25 MG, THREE TIMES A DAY AS NEEDED 0 25 MG TABLET
106956158 10695615 15 C ONE A DAY 2 ONE ONCE A DAY 0 1 DF QD
106956158 10695615 16 C FISH OIL FISH OIL 1 Oral 1000 MG, 1X/DAY 0 1000 MG CAPSULE QD
106956158 10695615 17 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 UNK 0
106956158 10695615 18 C BONIVA IBANDRONATE SODIUM 1 UNK 0
106956158 10695615 19 C ACETAMINOPHEN W/HYDROCODONE ACETAMINOPHENHYDROCODONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106956158 10695615 1 Neuropathy peripheral
106956158 10695615 2 Fibromyalgia
106956158 10695615 3 Neuroma
106956158 10695615 8 Sleep disorder
106956158 10695615 9 Gastric disorder
106956158 10695615 10 Atrial fibrillation
106956158 10695615 11 Migraine
106956158 10695615 12 Blood pressure abnormal
106956158 10695615 14 Pruritus
106956158 10695615 15 Supplementation therapy
106956158 10695615 16 Routine health maintenance

Outcome of event

Event ID CASEID OUTC COD
106956158 10695615 OT
106956158 10695615 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106956158 10695615 Animal bite
106956158 10695615 Anxiety
106956158 10695615 Blood glucose increased
106956158 10695615 Blood pressure decreased
106956158 10695615 Depressed mood
106956158 10695615 Drug ineffective
106956158 10695615 Dysstasia
106956158 10695615 Fall
106956158 10695615 Fractured coccyx
106956158 10695615 Gait disturbance
106956158 10695615 Hypoaesthesia
106956158 10695615 Intentional product use issue
106956158 10695615 Limb injury
106956158 10695615 Loss of consciousness
106956158 10695615 Lyme disease
106956158 10695615 Malaise
106956158 10695615 Middle insomnia
106956158 10695615 Mobility decreased
106956158 10695615 Neuroma
106956158 10695615 Overdose
106956158 10695615 Pain in extremity
106956158 10695615 Peripheral coldness
106956158 10695615 Renal disorder
106956158 10695615 Shock
106956158 10695615 Stress
106956158 10695615 Vomiting
106956158 10695615 Weight decreased

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

no results found

Therapies reported

no results found