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Amoxan adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Amoxan FDA safety alerts: No

Reported hospitalizations: 1

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

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5360781-X | Rhabdomyolysis
on Jun 06, 2007 Male patient from JAPAN , 30 years of age, was treated with Amoxan (View Usage). Patient experienced the following unwanted or unexpected effects: rhabdomyolysis. Amoxan dosage: Unk. During the same period patient was treated with SILECE (Unk) (View Silece Review and Silece Label ), COLONEL (Unk) (View Colonel Review and Colonel Label ), DOGMATYL (Unk) (View Dogmatyl Review and Dogmatyl Label ), MUCOSTA (Unk) (View Mucosta Review and Mucosta Label ), MYSLEE (Unk) (View Myslee Review and Myslee Label ), ZOLOFT (Unk) (View Zoloft Review and Zoloft Label ).

4730622-X | Retinal Depigmentation
Patient was taking Amoxan (View Usage). Patient had the following side effects: retinal depigmentation on Jul 05, 2005 from JAPAN Additional patient health information: Female patient , 50 years of age, was diagnosed with ill-defined disorder, depression (What is depression?) and. Amoxan dosage: Daily Dose: 20 Milligram(s). During the same period patient was treated with LUVOX (Daily Dose: 50 Milligram(s)) (View Luvox Review and Luvox Label ), SOLANAX (Daily Dose: 1.2 Milligram(s)) (View Solanax Review and Solanax Label ), MYSLEE (Daily Dose: 10 Milligram(s)) (View Myslee Review and Myslee Label ), KAMI KIHI TO (View Kami-kihi-to Review and Kami-kihi-to Label ).

4712848-4 | Retinal Depigmentation
Adverse event was reported on Jul 05, 2005 by a Female patient taking Amoxan (View Usage) (Dosage: Daily Dose: 20 Milligram(s)) was diagnosed with ill-defined disorder, depression (What is depression?) and. Location: JAPAN , 50 years of age, After Amoxan was administered, patient had the following side effects: retinal depigmentation. During the same period patient was treated with LUVOX (Daily Dose: 50 Milligram(s)) (View Luvox Review and Luvox Label ), SOLANAX (Daily Dose: 1.2 Milligram(s)) (View Solanax Review and Solanax Label ), MYSLEE (Daily Dose: 10 Milligram(s)) (View Myslee Review and Myslee Label ), KAMI KIHI TO (View Kami-kihi-to Review and Kami-kihi-to Label ).

4555495-X | Blood Creatine Phosphokinase Increased, Pyrexia
on May 11, 2004 Female patient from , weighting 119.0 lb, was diagnosed with depression (What is depression?) and was treated with Amoxan (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, pyrexia. Amoxan dosage: Daily Dose: 40 Milligram(s). During the same period patient was treated with DEPROMEL 25 (View Depromel 25 Review and Depromel 25 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 Amoxan 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 Amoxan quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Amoxan 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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)During the same period patient was treated with VALPROATE SODIUM, ZOLPIDEM TARTRATE, QUAZEPAM, ETIZOLAM, TOLEDOMIN, AMOXAN. Mirtazapine Side Effects Report: 6525059 ...

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Amoxan Reactions
Blood Creatine Phosphokinase Increased
Pyrexia
Retinal Depigmentation
Rhabdomyolysis
Amoxan 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 Amoxan 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!