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Fluitran adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Fluitran FDA safety alerts: No

Reported hospitalizations: 6

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

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6033163-5 | Vascular Pseudoaneurysm Ruptured
on Jan 06, 2009 Female patient from JAPAN , weighting 167.6 lb, was diagnosed with acute myocardial infarction and was treated with Fluitran (View Usage). Patient experienced the following unwanted or unexpected effects: vascular pseudoaneurysm ruptured. Fluitran dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), SENNOSIDE (View Sennoside Review and Sennoside Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), GASTER (View Gaster Review and Gaster Label ), GLYCINE 1.5% (View Glycine 1.5% Review and Glycine 1.5% Label ), SIGMART (View Sigmart Review and Sigmart Label ).

5967873-2 | Vascular Pseudoaneurysm Ruptured
Patient was taking Fluitran (View Usage). Patient had the following side effects: vascular pseudoaneurysm ruptured on Nov 20, 2008 from JAPAN Additional patient health information: Female patient , weighting 167.6 lb, . Fluitran dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), SENNOSIDE (View Sennoside Review and Sennoside Label ), LENDORM (View Lendorm Review and Lendorm Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), GLYCINE 1.5% (View Glycine 1.5% Review and Glycine 1.5% Label ), SIGMART (View Sigmart Review and Sigmart Label ).

5914116-1 | Liver Disorder, Pyrexia, Thrombocytopenia
Adverse event was reported on Sep 24, 2008 by a Male patient taking Fluitran (View Usage) (Dosage: ) was diagnosed with hypertension, supraventricular tachycardia, gastritis, angina pectoris, percutaneous coronary intervention and. Location: JAPAN , weighting 121.3 lb, After Fluitran was administered, patient had the following side effects: liver disorder, pyrexia, thrombocytopenia. During the same period patient was treated with LANIRAPID (View Lanirapid Review and Lanirapid Label ), DIOVAN (View Diovan Review and Diovan Label ), NORVASC (View Norvasc Review and Norvasc Label ), ADALAT (View Adalat Review and Adalat Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5689145-6 | Nephrolithiasis
on Mar 19, 2008 Male patient from JAPAN , weighting 165.3 lb, was diagnosed with hypertension, arterial thrombosis and was treated with Fluitran (View Usage). Patient experienced the following unwanted or unexpected effects: nephrolithiasis. Fluitran dosage: 2 Mg. During the same period patient was treated with DIOVAN (80 Mg) (View Diovan Review and Diovan Label ), ARTIST (10 Mg) (View Artist Review and Artist Label ), SEROQUEL (25 Mg) (View Seroquel Review and Seroquel Label ), CLOPIDOGREL (75 Mg) (View Clopidogrel Review and Clopidogrel Label ). Patient was hospitalized.


4609921-8 | Blood Pressure Decreased, Erythema, Shock
on Jan 17, 2005 Female patient from , 56 years of age, weighting 132.3 lb, was treated with Fluitran (View Usage). Patient had the following side effects: blood pressure decreased, erythema, shock. Fluitran dosage: 2 Mg, Qd. During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized.

4607810-6 | Blood Pressure Decreased, Erythema, Shock
Patient was taking Fluitran (View Usage). After Fluitran was administered, patient had the following side effects: blood pressure decreased, erythema, shock on Jan 17, 2005 from Additional patient health information: Female patient , 56 years of age, weighting 132.3 lb, . Fluitran dosage: 2 Mg, Qd. During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized.

4592782-3 | Blood Pressure Decreased, Lymphocyte Stimulation Test Positive, Rash Erythematous, Shock
Adverse event was reported on Jan 17, 2005 by a Female patient taking Fluitran (View Usage) (Dosage: Unk, Unk) was diagnosed with hypertension and. Location: , 56 years of age, weighting 132.3 lb, Patient experienced the following unwanted or unexpected effects: blood pressure decreased, lymphocyte stimulation test positive, rash erythematous, shock. During the same period patient was treated with DIOVAN (80 Mg/day) (View Diovan Review and Diovan Label ). Patient was hospitalized.

4563865-9 | Blood Pressure Decreased, Shock
on Jan 17, 2005 Female patient from , 56 years of age, was diagnosed with hypertension and was treated with Fluitran (View Usage). Patient had the following side effects: blood pressure decreased, shock. Fluitran dosage: . During the same period patient was treated with DIOVAN (80 Mg/day) (View Diovan Review and Diovan 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 Fluitran 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 Fluitran quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fluitran 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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Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

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Fluitran Reactions
Blood Pressure Decreased
Erythema
Liver Disorder
Lymphocyte Stimulation Test Positive
Nephrolithiasis
Pyrexia
Rash Erythematous
Shock
Thrombocytopenia
Vascular Pseudoaneurysm Ruptured
Fluitran 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 Fluitran 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!