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Levocarnitine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Levocarnitine FDA safety alerts: No

Reported hospitalizations: 1

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

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6743682-1 | Dyspnoea, Middle Insomnia, Poor Quality Sleep
on May 19, 2010 Male patient from FRANCE , 41 years of age, was diagnosed with mitochondrial myopathy acquired and was treated with Levocarnitine (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, middle insomnia, poor quality sleep. Levocarnitine dosage: Po. During the same period patient was treated with MNESIS (IDEBENONE) (View Mnesis (idebenone) Review and Mnesis (idebenone) Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

6542784-2 | International Normalised Ratio Increased
Patient was taking Levocarnitine (View Usage). Patient had the following side effects: international normalised ratio increased on Jan 06, 2010 from UNITED STATES Additional patient health information: Female patient , 70 years of age, was diagnosed with heart valve replacement and. Levocarnitine dosage: 2 Doses, Iv. During the same period patient was treated with WARFARIN SODIUM (5mg, 6 Days/wk, Oral) (View Warfarin Sodium Review and Warfarin Sodium Label ).

5951202-4 | Chills, Dyspnoea, Flushing, Headache, Infusion Related Reaction, Product Quality Issue
Adverse event was reported on Nov 11, 2008 by a Female patient taking Levocarnitine (View Usage) (Dosage: 1000mg Tid Iv Drip) was diagnosed with mitochondrial cytopathy and. Location: UNITED STATES , 57 years of age, weighting 160.0 lb, After Levocarnitine was administered, patient had the following side effects: chills, dyspnoea, flushing, headache (What is headache?), infusion related reaction, product quality issue.

4592759-8 | International Normalised Ratio Increased
on Feb 04, 2005 Male patient from , 33 years of age, was diagnosed with medical diet and was treated with Levocarnitine (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Levocarnitine dosage: 1000 Mg/day. During the same period patient was treated with ACENOCUMAROL (View Acenocumarol Review and Acenocumarol Label ).


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Levocarnitine Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

laurie   new england 

6:36pm on Monday, December 27th, 2010

Looking into side effects from levocarnitine. Believe my daughter may be experiencing them. Would ... read more »

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 Levocarnitine 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 Levocarnitine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Levocarnitine 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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Levocarnitine Reactions
Chills
Dyspnoea
Flushing
HeadacheWhat is Headache?
Infusion Related Reaction
International Normalised Ratio Increased
Middle Insomnia
Poor Quality Sleep
Product Quality Issue
Levocarnitine Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Levocarnitine adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!