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Lorzaar adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Lorzaar FDA safety alerts: No

Reported hospitalizations: 1

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

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5323452-1 | Contusion, Dystonia, Erythema, Fall, Lymphadenopathy, Nail Disorder, Oedema, Pruritus
on May 04, 2007 Male patient from GERMANY , 56 years of age, weighting 158.7 lb, was diagnosed with dystonia (What is dystonia?) and was treated with Lorzaar (View Usage). Patient experienced the following unwanted or unexpected effects: contusion, dystonia (What is dystonia?), erythema, fall (What is fall?), lymphadenopathy, nail disorder, oedema, pruritus. Lorzaar dosage: 50-0-0 Mg/day. During the same period patient was treated with HYDROCHLOROTHIAZIDE (12.5 Mg/day) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), UROXATRAL (0-0-10 Mg/day) (View Uroxatral Review and Uroxatral Label ), PRAVASTATIN (0-0-10 Mg/day) (View Pravastatin Review and Pravastatin Label ), AVODART (Every Second Day) (View Avodart Review and Avodart Label ), TEGRETOL (150 Mg, Bid) (View Tegretol Review and Tegretol Label ). Patient was hospitalized.

4798910-9 | Hypertension, Vitreous Haemorrhage
Patient was taking Lorzaar (View Usage). Patient had the following side effects: hypertension, vitreous haemorrhage on Sep 07, 2005 from GERMANY Additional patient health information: Female patient , 41 years of age, was diagnosed with nail tinea and. Lorzaar dosage: ^prophylactically^. During the same period patient was treated with NEURIUM /GFR/ (View Neurium /gfr/ Review and Neurium /gfr/ Label ), INSULIN BASAL (View Insulin Basal Review and Insulin Basal Label ), HUMALOG (View Humalog Review and Humalog Label ), LAMISIL (250 Mg, Qd) (View Lamisil Review and Lamisil Label ).

4763604-2 | Hypertension, Vitreous Haemorrhage
Adverse event was reported on Sep 07, 2005 by a Female patient taking Lorzaar (View Usage) (Dosage: ) was diagnosed with nail tinea and. Location: GERMANY , 41 years of age, After Lorzaar was administered, patient had the following side effects: hypertension, vitreous haemorrhage. During the same period patient was treated with NEURIUM /GFR/ (View Neurium /gfr/ Review and Neurium /gfr/ Label ), INSULIN BASAL (View Insulin Basal Review and Insulin Basal Label ), HUMALOG (View Humalog Review and Humalog Label ), LAMISIL (1 Df, Qd) (View Lamisil Review and Lamisil 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 Lorzaar 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 Lorzaar quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lorzaar 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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Lorzaar Reactions
Contusion
DystoniaWhat is Dystonia?
Erythema
FallWhat is Fall?
Hypertension
Lymphadenopathy
Nail Disorder
Oedema
Pruritus
Vitreous Haemorrhage
Lorzaar 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 Lorzaar 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!