Fludrocortisone Side Effects

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Fludrocortisone adverse events reported to FDA.

Have You Experienced unusual Fludrocortisone symptoms? PatientsVille.com collects and analyzes Fludrocortisone side effect and adverse reports submitted by Fludrocortisone users, such as .

Summary

FDA Adverse Reports: 4. View All

Fludrocortisone FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 4

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Often additional risks of using a medication, such as Fludrocortisone, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Fludrocortisone users, Learn more about unwanted side effects & find ways to reduce them. Browse Fludrocortisone Adverse Reports reported to FDA and participate in Fludrocortisone discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Fludrocortisone. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

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Fludrocortisone Adverse Effect Reports (FDA)

6699012-7 | Cardiac Failure, Condition Aggravated
on Apr 26, 2010 Male patient from UNITED STATES , 84 years of age, weighting 165.3 lb, was diagnosed with cardiac failure congestive and was treated with Fludrocortisone (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, condition aggravated. Fludrocortisone dosage: 0.2 Mg Bid Po. Patient was hospitalized.

6649740-4 | Oedema Peripheral
Patient was taking Fludrocortisone (View Usage). Patient had the following side effects: oedema peripheral on Mar 24, 2010 from UNITED STATES Additional patient health information: Male patient , 60 years of age, weighting 175.0 lb, was diagnosed with pain (What is pain?) and. Fludrocortisone dosage: 0.1 Mg Every Day Po. During the same period patient was treated with GABAPENTIN (100 Mg Tid Po) (View Gabapentin Review and Gabapentin Label ). Patient was hospitalized.

6297528-9 | Asthenia, Hypokalaemia
Adverse event was reported on Aug 04, 2009 by a Male patient taking Fludrocortisone (View Usage) (Dosage: 0.1 Mg Every Day Po) was diagnosed with adrenal insufficiency, hypertension and. Location: UNITED STATES , 79 years of age, weighting 154.1 lb, After Fludrocortisone was administered, patient had the following side effects: asthenia, hypokalaemia. During the same period patient was treated with HYDROCHLOROTHIAZIDE (25 Mg Every Day Po) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

4654984-7 | Cardiac Disorder, Dyspnoea, Pruritus, Swollen Tongue, Tracheal Oedema, Urticaria
on Apr 18, 2005 Male patient from , 67 years of age, weighting 270.0 lb, was diagnosed with hypotension and was treated with Fludrocortisone (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac disorder, dyspnoea, pruritus, swollen tongue, tracheal oedema, urticaria. Fludrocortisone dosage: 0.1 Mg Qday Po. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), FLOMAX (View Flomax Review and Flomax Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NEXIUM (View Nexium Review and Nexium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), XANAX (View Xanax Review and Xanax Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ). Patient was hospitalized.

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Fludrocortisone risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Fludrocortisone quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fludrocortisone use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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	Yes, Minor
	No

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FLUDROCORTISONE Side Effects

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Fludrocortisone Reactions

Asthenia
Cardiac Disorder
Cardiac Failure
Condition Aggravated
Dyspnoea
Hypokalaemia
Oedema Peripheral
Pruritus
Swollen Tongue
Tracheal Oedema
Urticaria

FLUDROCORTISONE Side Effects

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Fludrocortisone adverse events reported to FDA.

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Fludrocortisone Adverse Effect Reports (FDA)

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Fludrocortisone Reactions