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
124475855 12447585 5 F 2016 20160909 20160608 20160914 EXP US-PFIZER INC-2016288377 PFIZER 90.00 YR F Y 72.00000 KG 20160914 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
124475855 12447585 1 PS PREMARIN ESTROGENS, CONJUGATED 1 Oral UNK, HIGHER DOSE 4782 TABLET
124475855 12447585 2 SS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, DAILY J53551AN 4782 .3 MG TABLET
124475855 12447585 3 SS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, 6 TIMES A WEEK 4782 .3 MG TABLET
124475855 12447585 4 SS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, 5 TIMES A WEEK 4782 .3 MG TABLET
124475855 12447585 5 SS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, 5 TIMES A WEEK 4782 .3 MG TABLET
124475855 12447585 6 C PREMARIN ESTROGENS, CONJUGATED 1 UNK, (0.625 APPLIED SEVERAL TIMES) 0
124475855 12447585 7 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 0.025 MG, 1X/DAY 0 .025 MG QD
124475855 12447585 8 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 10 MG, 1X/DAY 0 10 MG QD
124475855 12447585 9 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 20 MG, 1X/DAY 0 20 MG QD
124475855 12447585 10 C RANITIDINE. RANITIDINE 1 Oral 150 MG, 1X/DAY 0 150 MG QD
124475855 12447585 11 C ROPINIROLE HYDROCHLORIDE. ROPINIROLE HYDROCHLORIDE 1 1 MG, UNK 0 1 MG
124475855 12447585 12 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
124475855 12447585 13 C LOVASTATIN. LOVASTATIN 1 0
124475855 12447585 14 C MEVACOR LOVASTATIN 1 Oral 20 MG, 1X/DAY 0 20 MG QD
124475855 12447585 15 C HCTZ HYDROCHLOROTHIAZIDE 1 UNK 0
124475855 12447585 16 C ATIVAN LORAZEPAM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124475855 12447585 1 Hormone replacement therapy
124475855 12447585 6 Hormone replacement therapy
124475855 12447585 7 Thyroid disorder
124475855 12447585 8 Cardiac disorder
124475855 12447585 9 Abdominal discomfort
124475855 12447585 10 Abdominal discomfort
124475855 12447585 14 Blood cholesterol

Outcome of event

Event ID CASEID OUTC COD
124475855 12447585 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124475855 12447585 Anxiety
124475855 12447585 Asthenia
124475855 12447585 Blood pressure increased
124475855 12447585 Bone pain
124475855 12447585 Fatigue
124475855 12447585 Headache
124475855 12447585 Hyperhidrosis
124475855 12447585 Intentional product use issue
124475855 12447585 Lethargy
124475855 12447585 Malaise
124475855 12447585 Nausea
124475855 12447585 Pain
124475855 12447585 Sleep disorder

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
124475855 12447585 3 201603 0
124475855 12447585 4 201604 0
124475855 12447585 5 201605 0