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Eflornithine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Eflornithine FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 2

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

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5609469-8 | Aspiration, Blood Pressure Decreased, Confusional State, Convulsion, Delirium, Heart Rate Increased, Infusion Site Cellulitis, Loss Of Consciousness
on Jan 28, 2008 Female patient from UGANDA , 26 years of age, weighting 111.8 lb, was diagnosed with african trypanosomiasis and was treated with Eflornithine (View Usage). Patient experienced the following unwanted or unexpected effects: aspiration, blood pressure decreased, confusional state, convulsion, delirium, heart rate increased, infusion site cellulitis, loss of consciousness. Eflornithine dosage: .

5605959-2 | Convulsion
Patient was taking Eflornithine (View Usage). Patient had the following side effects: convulsion on Jan 23, 2008 from UGANDA Additional patient health information: Female patient , 26 years of age, weighting 111.8 lb, was diagnosed with cellulitis (What is cellulitis?) and. Eflornithine dosage: . During the same period patient was treated with CEFTRIAXONE (View Ceftriaxone Review and Ceftriaxone Label ).

5570876-3 | Headache, Vomiting
Adverse event was reported on Dec 18, 2007 by a Female patient taking Eflornithine (View Usage) (Dosage: ) . Location: UGANDA , 31 years of age, weighting 93.04 lb, After Eflornithine was administered, patient had the following side effects: headache (What is headache?), vomiting. During the same period patient was treated with NIFURTIMOX (View Nifurtimox Review and Nifurtimox Label ). Patient was hospitalized.

5545672-3 | Cerebrovascular Accident, Headache, Vomiting
on Dec 04, 2007 Female patient from UGANDA , 31 years of age, weighting 93.04 lb, was treated with Eflornithine (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, headache (What is headache?), vomiting. Eflornithine dosage: . During the same period patient was treated with NIFURTIMOX (View Nifurtimox Review and Nifurtimox Label ). Patient was hospitalized.


5530516-6 | Headache, Vomiting
on Nov 26, 2007 Female patient from UGANDA , 31 years of age, weighting 93.04 lb, was diagnosed with african trypanosomiasis, headache (What is headache?) and was treated with Eflornithine (View Usage). Patient had the following side effects: headache (What is headache?), vomiting. Eflornithine dosage: . During the same period patient was treated with NIFURTIMOX (View Nifurtimox Review and Nifurtimox Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).


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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 Eflornithine 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 Eflornithine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Eflornithine 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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Eflornithine Reactions
Aspiration
Blood Pressure Decreased
Cerebrovascular Accident
Confusional State
Convulsion
Death
Delirium
HeadacheWhat is Headache?
Heart Rate Increased
Infusion Site Cellulitis
Loss Of Consciousness
Vomiting
Eflornithine 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 Eflornithine 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!