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Alora adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Alora FDA safety alerts: No

Reported hospitalizations: 2

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

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6920979-3 | Blood Prolactin Increased, Galactorrhoea, Gynaecomastia, Prolactinoma
on Aug 02, 2010 Male patient from BRAZIL , 42 years of age, was treated with Alora (View Usage). Patient experienced the following unwanted or unexpected effects: blood prolactin increased, galactorrhoea, gynaecomastia, prolactinoma. Alora dosage: 10 Mg Im Every 15 Days.

5702905-8 | Scratch
Patient was taking Alora (View Usage). Patient had the following side effects: scratch on Apr 10, 2008 from UNITED STATES Additional patient health information: Female patient , 63 years of age, weighting 145.0 lb, . Alora dosage: 00.1 2x Weekly.

5660290-4 | Deep Vein Thrombosis, Oedema Peripheral
Adverse event was reported on Sep 19, 2007 by a Female patient taking Alora (View Usage) (Dosage: 1 Patch, 2/week, Transdermal ; 1 Patch, 2/week, Transdermal) . Location: UNITED STATES , 48 years of age, After Alora was administered, patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), oedema peripheral.

5273533-6 | Blister
on Mar 21, 2007 Male patient from UNITED STATES , 50 years of age, weighting 190.0 lb, was treated with Alora (View Usage). Patient experienced the following unwanted or unexpected effects: blister. Alora dosage: 1 Patch Twice Weekly At Least 2 Years. During the same period patient was treated with CARDIZEM (View Cardizem Review and Cardizem Label ), BENICAR HCT (View Benicar Hct Review and Benicar Hct Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LUNETSA (View Lunetsa Review and Lunetsa Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), PRILOSEC (View Prilosec Review and Prilosec Label ).


4976931-0 | Breast Cancer Female, Breast Disorder Female, Breast Pain, Breast Swelling, Breast Tenderness, Hypertrophy Breast
on Apr 05, 2006 Female patient from UNITED STATES , 63 years of age, was treated with Alora (View Usage). Patient had the following side effects: breast cancer female, breast disorder female, breast pain, breast swelling, breast tenderness, hypertrophy breast. Alora dosage: 1 Patch, 2/week, Transdermal. During the same period patient was treated with MEDROXYPROGESTERONE (View Medroxyprogesterone Review and Medroxyprogesterone Label ), VICOPROFEN (View Vicoprofen Review and Vicoprofen Label ), ATIVAN (View Ativan Review and Ativan Label ).

4972259-3 | Asthenia, Brain Stem Infarction, Ear Discomfort, Hypertension, Hypoaesthesia, Menorrhagia, Vertigo
Patient was taking Alora (View Usage). After Alora was administered, patient had the following side effects: asthenia, brain stem infarction, ear discomfort, hypertension, hypoaesthesia, menorrhagia, vertigo on Oct 14, 2005 from UNITED STATES Additional patient health information: Female patient , 65 years of age, weighting 125.0 lb, was diagnosed with osteoporosis (What is osteoporosis?) and. Alora dosage: See Image, Transermal. During the same period patient was treated with DIOVAN (View Diovan Review and Diovan Label ), NORVASC (View Norvasc Review and Norvasc Label ). Patient was hospitalized.

4787272-9 | Lymphangioleiomyomatosis
Adverse event was reported on Sep 21, 2005 by a Female patient taking Alora (View Usage) (Dosage: 1 Month, Transdermal) . Location: SPAIN , 59 years of age, Patient experienced the following unwanted or unexpected effects: lymphangioleiomyomatosis. During the same period patient was treated with PROGESTERONE TRANSDERMAL PATCH (View Progesterone Transdermal Patch Review and Progesterone Transdermal Patch 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 Alora 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 Alora quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Alora 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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Alora Reactions
Asthenia
Blister
Blood Prolactin Increased
Brain Stem Infarction
Breast Cancer Female
Breast Disorder Female
Breast Pain
Breast Swelling
Breast Tenderness
Deep Vein ThrombosisWhat is Deep vein thrombosis?
Ear Discomfort
Galactorrhoea
Gynaecomastia
Hypertension
Hypertrophy Breast
Hypoaesthesia
Lymphangioleiomyomatosis
Menorrhagia
Oedema Peripheral
Prolactinoma
Scratch
Vertigo
Alora 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 Alora 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!