Levodopa Side Effects

If You had Levodopa side effect, You are not alone. Other patients reported side effects.

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Levodopa adverse events reported to FDA.

Have You Experienced unusual Levodopa symptoms? PatientsVille.com collects and analyzes Levodopa side effect and adverse reports submitted by Levodopa users, such as LOW WHITE BLOOD CELL COUNT |.

Summary

FDA Adverse Reports: 4. View All

Levodopa FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Levodopa, 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 Levodopa users, Learn more about unwanted side effects & find ways to reduce them. Browse Levodopa Adverse Reports reported to FDA and participate in Levodopa discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Levodopa. 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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Levodopa Adverse Effect Reports (FDA)

6941416-9 | Dopamine Dysregulation Syndrome
on Aug 11, 2010 Male patient from NETHERLANDS , 43 years of age, was diagnosed with parkinson's disease (What is parkinson's disease?), psychomotor hyperactivity, back pain (What is back pain?) and was treated with Levodopa (View Usage). Patient experienced the following unwanted or unexpected effects: dopamine dysregulation syndrome. Levodopa dosage: . During the same period patient was treated with ROPINIROLE (View Ropinirole Review and Ropinirole Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ). Patient was hospitalized.

6914861-5 | Condition Aggravated, Dyskinesia
Patient was taking Levodopa (View Usage). Patient had the following side effects: condition aggravated, dyskinesia on Aug 04, 2010 from UNITED STATES Additional patient health information: Male patient , 82 years of age, . Levodopa dosage: . Patient was hospitalized and became disabled.

5101447-0 | Cardiac Arrest
Adverse event was reported on Sep 04, 2006 by a Male patient taking Levodopa (View Usage) (Dosage: Unk) was diagnosed with parkinson's disease (What is parkinson's disease?), pancreatic carcinoma and. Location: ITALY , 63 years of age, After Levodopa was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?). During the same period patient was treated with GEMCITABINA (Unk) (View Gemcitabina Review and Gemcitabina Label ), ELOXATIN (Unk) (View Eloxatin Review and Eloxatin Label ).

5006437-4 | Dyspnoea, Pleural Fibrosis
on May 16, 2006 Male patient from AUSTRALIA , 48 years of age, was diagnosed with parkinson's disease (What is parkinson's disease?) and was treated with Levodopa (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, pleural fibrosis. Levodopa dosage: . During the same period patient was treated with CABASER (8 Mg, Daily) (View Cabaser Review and Cabaser Label ), COMTAN (View Comtan Review and Comtan 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 Levodopa 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 Levodopa quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Levodopa 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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	Effective
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LEVODOPA Side Effects

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Levodopa adverse events reported to FDA.

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Levodopa Adverse Effect Reports (FDA)

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Cardiac Arrest	What is Cardiac arrest?
Condition Aggravated
Dopamine Dysregulation Syndrome
Dyskinesia
Dyspnoea
Pleural Fibrosis

LEVODOPA Side Effects

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Detailed Reporting will help others get complete information and find alternative treatments to avoid or reduce side effects associated with it.

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Levodopa adverse events reported to FDA.

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Levodopa Adverse Effect Reports (FDA)

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Levodopa Reactions