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Famcyclovir adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Famcyclovir FDA safety alerts: No

Reported hospitalizations: 2

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

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4821836-9 | Blood Creatinine Increased, Blood Potassium Increased, Blood Urea Increased, Dehydration, Disorientation, Pruritus, Vomiting
on Jun 02, 2005 Female patient from UNITED STATES , 84 years of age, was treated with Famcyclovir (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood potassium increased, blood urea increased, dehydration, disorientation, pruritus, vomiting. Famcyclovir dosage: 500 Mg, Tid. During the same period patient was treated with POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), LESCOL XL (View Lescol Xl Review and Lescol Xl Label ), LASIX (View Lasix Review and Lasix Label ), NEXIUM (View Nexium Review and Nexium Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), AMBIEN (View Ambien Review and Ambien Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ). Patient was hospitalized.

4688695-9 | Carotid Artery Stenosis, Dizziness, Hypovolaemia, Oral Intake Reduced
Patient was taking Famcyclovir (View Usage). Patient had the following side effects: carotid artery stenosis, dizziness (What is dizziness?), hypovolaemia, oral intake reduced on May 24, 2004 from Additional patient health information: Female patient , 71 years of age, was diagnosed with herpes zoster and. Famcyclovir dosage: 500 Mg, Tid. During the same period patient was treated with MIACALCIN (View Miacalcin Review and Miacalcin Label ), MOBIC (View Mobic Review and Mobic Label ), HYDROCHLOROTHIAZIDE (Not Reported) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), CELEXA (View Celexa Review and Celexa Label ), MIRALAX (View Miralax Review and Miralax Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid 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 Famcyclovir 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 Famcyclovir quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Famcyclovir 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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Famcyclovir Reactions
Blood Creatinine Increased
Blood Potassium Increased
Blood Urea Increased
Carotid Artery Stenosis
Dehydration
Disorientation
DizzinessWhat is Dizziness?
Hypovolaemia
Oral Intake Reduced
Pruritus
Vomiting
Famcyclovir 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 Famcyclovir 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!