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
125084202 12508420 2 F 20160701 20160629 20160706 EXP FI-PFIZER INC-2016320304 PFIZER TUMPULA O, ET AL. SEVERE HEADACHE DURING A NIGHT. DUODECIM. 2016;132:1131 63.00 YR M Y 0.00000 20160706 OT FI FI

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
125084202 12508420 1 PS RAMIPRIL. RAMIPRIL 1 Oral 2.5 MG, DAILY U 19901 2.5 MG
125084202 12508420 2 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Oral 10 MG, DAILY U 0 10 MG TABLET
125084202 12508420 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 5 MG, DAILY U 0 5 MG
125084202 12508420 4 SS BISOPROLOL BISOPROLOL 1 Unknown 2.5 MG, DAILY U 0 2.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125084202 12508420 3 Fibromyalgia

Outcome of event

Event ID CASEID OUTC COD
125084202 12508420 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125084202 12508420 Eyelid ptosis
125084202 12508420 Fatigue
125084202 12508420 Gaze palsy
125084202 12508420 Headache
125084202 12508420 Hyponatraemia
125084202 12508420 Muscular weakness
125084202 12508420 Musculoskeletal stiffness
125084202 12508420 Nausea
125084202 12508420 Photophobia
125084202 12508420 Pituitary tumour benign
125084202 12508420 Seizure
125084202 12508420 Visual impairment

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

no results found

Therapies reported

no results found