The Safety Rates Drug Report

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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
125184572 12518457 2 F 20160628 20160630 20160705 EXP FI-BAUSCH-BL-2016-015278 BAUSCH AND LOMB TUMPULA O, ROSENGARD-BARLUND M, TUOMI T, LINDSBERG P. SEVERE HEADACHE DURING A NIGHT. DUODECIM FORTHCOMING. 2016;132:1131:. 63.00 YR M Y 0.00000 20160705 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
125184572 12518457 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070 5 MG QD
125184572 12518457 2 SS ROSUVASTATIN CALCIUM. ROSUVASTATIN CALCIUM 1 Oral U 0 10 MG TABLET QD
125184572 12518457 3 SS RAMIPRIL. RAMIPRIL 1 Oral U 0 2.5 MG QD
125184572 12518457 4 SS BISOPROLOL SALT NOT SPECIFIED BISOPROLOL 1 Unknown U 0 2.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125184572 12518457 1 Fibromyalgia
125184572 12518457 2 Product used for unknown indication
125184572 12518457 3 Product used for unknown indication
125184572 12518457 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125184572 12518457 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125184572 12518457 Eyelid ptosis
125184572 12518457 Fatigue
125184572 12518457 Gaze palsy
125184572 12518457 Headache
125184572 12518457 Hyponatraemia
125184572 12518457 Muscular weakness
125184572 12518457 Musculoskeletal stiffness
125184572 12518457 Nausea
125184572 12518457 Photophobia
125184572 12518457 Pituitary tumour benign
125184572 12518457 Seizure
125184572 12518457 Visual impairment

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

no results found

Therapies reported

no results found