This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Florinef (Fludrocortisone) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.
Reports by Event Outcome
All Cases (4)
Death (1)
Life Threatening Events (1)
Reports by Reaction Type
Orthostatic Hypotension (2),
Femur Fracture (1),
Haemorrhage (1),
Headache (1),
Loss of Consciousness (1),
Multiple Sclerosis Relapse (1),
Death (1),
Haematocrit Decreased (1),
RED Blood Cell Count Decreased (1),
Cardiac Failure Congestive (1),
Blood Glucose Increased (1),
International Normalised Ratio Increased (1)
Possible Florinef side effects in
Reported by a pharmacist from Japan on 2012-08-23
Patient:
Reactions: Femur Fracture, Haematuria, Platelet Count Decreased, Orthostatic Hypotension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Florinef
Dosage: 0.1 mg, qd
Administration route: Oral
Menesit Tablets - 250
Dosage: daily dosage unknown
Administration route: Oral
Indication: Parkinson's Disease
Dops
Dosage: 200 mg, tid
Administration route: Oral
Motilium
Dosage: 10 mg, tid
Administration route: Oral
Other drugs received by patient: Furosemide; FP (Selegiline Hydrochloride); Metligine
Possible Florinef side effects in 98 year old male
Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-23
Patient: 98 year old male, weighing 81.5 kg (179.3 pounds)
Reactions: Swelling, Hypertension
Drug(s) suspected as cause:
Florinef
Dosage: 0.1mg once daily po
Administration route: Oral
Midodrine Hydrochloride
Dosage: 10mg three times daily po
Administration route: Oral
Possible Florinef side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-28
Patient: female
Reactions: Orthostatic Hypotension, Headache, Multiple Sclerosis Relapse, Loss of Consciousness, Haemoglobin Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Glucose Increased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Atacand
Dosage: unk
Administration route: Oral
Indication: Hypertension
End date: 2009-03-01
Florinef
Verapamil HCL
Dosage: unk
Administration route: Oral
Indication: Hypertension
End date: 2009-03-01
Quinapril Hydrochloride
Dosage: unk
Administration route: Oral
Indication: Hypertension
End date: 2009-03-01
Rebif
Dosage: 44 ug, unk
Indication: Multiple Sclerosis
Start date: 2007-11-29
Other drugs received by patient: Metformin
Possible Florinef side effects in 86 year old female
Reported by a consumer/non-health professional from United States on 2012-05-09
Patient: 86 year old female
Reactions: Death, Haemorrhage, International Normalised Ratio Increased, Anaemia, Deep Vein Thrombosis, Cardiac Failure Congestive
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Coumadin
Dosage: 2.5 mg of coumadin 3 days a week and 5 mg on the other 4 days of the week.
Indication: Deep Vein Thrombosis
Florinef
Dosage: taken off:20apr12
Aspirin
Other drugs received by patient: Cozaar; Coenzyme Q10; Vitamin D; Simvastatin; Insulin; Pepcid; Vitamin B Complex CAP; Iron Supplement
|