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
109823496 10982349 6 F 201602 20160715 20150403 20160728 EXP US-PFIZER INC-2015017480 PFIZER 92.00 YR F Y 65.31000 KG 20160728 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
109823496 10982349 1 PS LYRICA PREGABALIN 1 Oral 200 MG, 2X/DAY 21446 200 MG CAPSULE, HARD BID
109823496 10982349 2 SS LYRICA PREGABALIN 1 Oral 200 MG, 2X/DAY J82634 21446 200 MG CAPSULE, HARD BID
109823496 10982349 3 SS LYRICA PREGABALIN 1 Oral UNK, 2X/DAY 21446 CAPSULE, HARD BID
109823496 10982349 4 SS LYRICA PREGABALIN 1 Oral 200 MG, UNK 21446 200 MG CAPSULE, HARD
109823496 10982349 5 C ALBUTEROL. ALBUTEROL 1 Nasal 2.5 MG PER 3 ML, NEBULIZATION, Q4-6HR AS NEEDED 0
109823496 10982349 6 C ALBUTEROL. ALBUTEROL 1 0
109823496 10982349 7 C ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral 2 DF, DAILY 0 2 DF TABLET
109823496 10982349 8 C ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral 1 DF, DAILY 0 1 DF TABLET
109823496 10982349 9 C DICLOFENAC POTASSIUM. DICLOFENAC POTASSIUM 1 Oral 50 MG ORAL TABLET 3 TIMES A DAY (TID), PRN 0 150 MG TABLET
109823496 10982349 10 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, DAILY 0 20 MG PROLONGED-RELEASE CAPSULE
109823496 10982349 11 C TRAMADOL. TRAMADOL 1 Oral 200 MG, AS NEEDED (50 MG, 4 TIMES A DAY WHEN SHE NEEDS IT) 0 200 MG TABLET
109823496 10982349 12 C TRAMADOL. TRAMADOL 1 Oral 50 MG, AS NEEDED 0 50 MG TABLET
109823496 10982349 13 C AMBIEN ZOLPIDEM TARTRATE 1 Oral 5 MG, AS NEEDED (QHS (EACH NIGHT AT BEDTIME)) 0 5 MG TABLET
109823496 10982349 14 C CELEXA CITALOPRAM HYDROBROMIDE 1 Oral 20 MG, DAILY 0 20 MG TABLET
109823496 10982349 15 C PREDNISONE. PREDNISONE 1 Oral 40 MG, 1X/DAY 0 40 MG TABLET QD
109823496 10982349 16 C PREDNISONE. PREDNISONE 1 Oral 30 MG, 1X/DAY 0 30 MG TABLET QD
109823496 10982349 17 C PREDNISONE. PREDNISONE 1 Oral 20 MG, 1X/DAY 0 20 MG TABLET QD
109823496 10982349 18 C PREDNISONE. PREDNISONE 1 Oral 10 MG, 1X/DAY 0 10 MG TABLET QD
109823496 10982349 19 C AZELASTINE AZELASTINE 1 Nasal 2 SPRAYS EACH NOSTRIL, 2X/DAY 0 4 DF BID
109823496 10982349 20 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 10 MG, DAILY 0 10 MG TABLET
109823496 10982349 21 C DULCOLAX NOS BISACODYL OR DOCUSATE SODIUM 1 Oral DOCUSATE-50 MG, SENNA-8.6 MG ) (ONCE A DAY IN THE EVENING) 0 1 DF TABLET QD
109823496 10982349 22 C LEVAQUIN LEVOFLOXACIN 1 Oral 500 MG, 1X/DAY (500 MG TABLET Q 24HR, 10 DAY(S) 10 TABLET AND 7 DAY(S) 7 TABLET) 0 500 MG TABLET QD
109823496 10982349 23 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 Oral 20 MEQ, 2X/DAY 0 20 MEQ PROLONGED-RELEASE TABLET BID
109823496 10982349 24 C POLYETHYLENE GLYCOL 3350. POLYETHYLENE GLYCOL 3350 1 Oral 17 G, 1X/DAY 0 17 G QD
109823496 10982349 25 C VISTARIL HYDROXYZINE PAMOATE 1 Oral 100 MG, AS NEEDED (25 MG QID PRN) 0 100 MG CAPSULE
109823496 10982349 26 C MULTIVITAMINS VITAMINS 1 Oral 1 DF, DAILY 0 1 DF TABLET
109823496 10982349 27 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 20 MG, 1X/DAY 0 20 MG QD
109823496 10982349 28 C LAXATIVE UNSPECIFIED INGREDIENT 1 UNK, 1X/DAY (CAP FULL EVERY MORNING) 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109823496 10982349 1 Neuralgia
109823496 10982349 2 Neuropathy peripheral
109823496 10982349 3 Pain
109823496 10982349 5 Wheezing
109823496 10982349 6 Dyspnoea
109823496 10982349 9 Pain
109823496 10982349 11 Pain
109823496 10982349 13 Sleep disorder
109823496 10982349 25 Pruritus
109823496 10982349 27 Neuralgia
109823496 10982349 28 Constipation

Outcome of event

Event ID CASEID OUTC COD
109823496 10982349 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109823496 10982349 Body height decreased
109823496 10982349 Bronchitis
109823496 10982349 Burning sensation
109823496 10982349 Chills
109823496 10982349 Condition aggravated
109823496 10982349 Cough
109823496 10982349 Drug dose omission
109823496 10982349 Drug ineffective
109823496 10982349 Fall
109823496 10982349 Fatigue
109823496 10982349 Foot fracture
109823496 10982349 Gingival swelling
109823496 10982349 Hyperhidrosis
109823496 10982349 Hypersensitivity
109823496 10982349 Hypoacusis
109823496 10982349 Influenza
109823496 10982349 Insomnia
109823496 10982349 Intentional product misuse
109823496 10982349 Malaise
109823496 10982349 Nasal congestion
109823496 10982349 Nausea
109823496 10982349 Pain
109823496 10982349 Pain in extremity
109823496 10982349 Protein total decreased
109823496 10982349 Sebaceous carcinoma
109823496 10982349 Spinal deformity
109823496 10982349 Swollen tongue
109823496 10982349 Viral upper respiratory tract infection
109823496 10982349 Weight increased

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
109823496 10982349 2 20141028 0