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Droxia adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Droxia FDA safety alerts: 2006

Reported hospitalizations: 1

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

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6163849-3 | Alopecia, Asthenia, Balance Disorder, Confusional State, Depression, Hot Flush, Loss Of Consciousness, Rash, Vomiting
on Apr 07, 2008 Female patient from UNITED STATES , 89 years of age, weighting 114.6 lb, was diagnosed with platelet count increased and was treated with Droxia (View Usage). Patient experienced the following unwanted or unexpected effects: alopecia, asthenia, balance disorder, confusional state, depression (What is depression?), hot flush, loss of consciousness, rash (What is rash?), vomiting. Droxia dosage: Reduced To 300mg Daily,reduced To 200mg Daily For About6months - 1year.atpresent Takes 400mg Daily. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

5713128-0 | Alopecia, Rash, Vomiting
Patient was taking Droxia (View Usage). Patient had the following side effects: alopecia, rash (What is rash?), vomiting on Jan 10, 2008 from UNITED STATES Additional patient health information: Female patient , 89 years of age, weighting 114.6 lb, was diagnosed with platelet count increased and. Droxia dosage: Reduced To 300mg Daily,reduced To 200mg Daily For About6months - 1year.atpresent Takes 400mg Daily. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

4962292-X | Dysuria
Adverse event was reported on Jul 25, 2005 by a Male patient taking Droxia (View Usage) (Dosage: ) . Location: UNITED STATES , 30 years of age, After Droxia was administered, patient had the following side effects: dysuria. During the same period patient was treated with ZOLOFT (View Zoloft Review and Zoloft Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), PREVACID (View Prevacid Review and Prevacid Label ), PHENERGAN HCL (View Phenergan Hcl Review and Phenergan Hcl Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), OXYCODONE (View Oxycodone Review and Oxycodone Label ), LORATADINE (View Loratadine Review and Loratadine 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 Droxia 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 Droxia quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Droxia 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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Droxia Reactions
Alopecia
Asthenia
Balance Disorder
Confusional State
DepressionWhat is Depression?
Dysuria
Hot Flush
Loss Of Consciousness
RashWhat is Rash?
Vomiting
Droxia 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 Droxia 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!