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Transfusions adverse events reported to FDA.

Have You Experienced unusual Transfusions symptoms? PatientsVille.com collects and analyzes Transfusions side effect and adverse reports submitted by Transfusions users, such as I became very anemic - and have|.

Summary

FDA Adverse Reports: 4. View All

Transfusions FDA safety alerts: No

Reported hospitalizations: 1

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I became very anemic - and have

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

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5408030-8 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Chloride Increased, Blood Creatinine Increased, Blood Glucose Increased, Blood Phosphorus Increased, Blood Thyroid Stimulating Hormone Increased, Blood Urea Increased
on Aug 03, 2007 Female patient from UNITED STATES , 43 years of age, was diagnosed with iron overload and was treated with Transfusions (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood chloride increased, blood creatinine increased, blood glucose increased, blood phosphorus increased, blood thyroid stimulating hormone increased, blood urea increased. Transfusions dosage: . During the same period patient was treated with EXJADE (1500 Mg, Qd) (View Exjade Review and Exjade Label ), LOVENOX (150 Mg, Unk) (View Lovenox Review and Lovenox Label ), LISINOPRIL (10 Mg, Qd) (View Lisinopril Review and Lisinopril Label ), AMITRIPTYLINE HCL (25 Mg, Unk) (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), SIMVASTATIN (20 Mg, Qd) (View Simvastatin Review and Simvastatin Label ), ESTRADERM (0.05 Mg, Qd) (View Estraderm Review and Estraderm Label ).

5404215-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Chloride Increased, Blood Creatinine Increased, Blood Glucose Increased, Blood Phosphorus Increased, Blood Thyroid Stimulating Hormone Increased, Blood Urea Increased
Patient was taking Transfusions (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood chloride increased, blood creatinine increased, blood glucose increased, blood phosphorus increased, blood thyroid stimulating hormone increased, blood urea increased on Jul 27, 2007 from UNITED STATES Additional patient health information: Female patient , 43 years of age, was diagnosed with iron overload and. Transfusions dosage: . During the same period patient was treated with EXJADE (1500 Mg, Qd) (View Exjade Review and Exjade Label ), LOVENOX (150 Mg, Unk) (View Lovenox Review and Lovenox Label ), LISINOPRIL (10 Mg, Qd) (View Lisinopril Review and Lisinopril Label ), AMITRIPTYLINE HCL (25 Mg, Unk) (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), SIMVASTATIN (20 Mg, Qd) (View Simvastatin Review and Simvastatin Label ), ESTRADERM (0.05 Mg, Qd) (View Estraderm Review and Estraderm Label ).

5087375-8 | Anaemia, Bone Marrow Failure, Haemoglobin Decreased, Neutropenia, Red Blood Cell Count Decreased, Thrombocytopenia
Adverse event was reported on Aug 07, 2006 by a Male patient taking Transfusions (View Usage) (Dosage: ) . Location: BRAZIL , 73 years of age, After Transfusions was administered, patient had the following side effects: anaemia, bone marrow failure, haemoglobin decreased, neutropenia, red blood cell count decreased, thrombocytopenia. During the same period patient was treated with DESFERAL (1 Application Every Month) (View Desferal Review and Desferal Label ), BACTRIM (Sometimes Monday And Tuesday) (View Bactrim Review and Bactrim Label ).

4606117-0 | Anti-hbc Antibody, Blood Bilirubin Increased, Hepatectomy, Hepatic Neoplasm Malignant Resectable, Hepatitis B Antibody, Hepatitis C Antibody Positive, Hepatitis C Rna Positive, Osteoporotic Fracture, Transaminases Increased
on Feb 28, 2005 Female patient from , 63 years of age, was diagnosed with thalassaemia beta and was treated with Transfusions (View Usage). Patient experienced the following unwanted or unexpected effects: anti-hbc antibody, blood bilirubin increased, hepatectomy, hepatic neoplasm malignant resectable, hepatitis b antibody, hepatitis c antibody positive, hepatitis c rna positive, osteoporotic fracture, transaminases increased. Transfusions dosage: . During the same period patient was treated with DESFERRIOXAMINE MESYLATE (View Desferrioxamine Mesylate Review and Desferrioxamine Mesylate 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 Transfusions 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 Transfusions quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Transfusions 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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Transfusions Reactions
Alanine Aminotransferase Increased
Anaemia
Anti-hbc Antibody
Aspartate Aminotransferase Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Chloride Increased
Blood Creatinine Increased
Blood Glucose Increased
Blood Phosphorus Increased
Blood Thyroid Stimulating Hormone Increased
Blood Urea Increased
Bone Marrow Failure
Haemoglobin Decreased
Hepatectomy
Hepatic Neoplasm Malignant Resectable
Hepatitis B Antibody
Hepatitis C Antibody Positive
Hepatitis C Rna Positive
Neutropenia
Osteoporotic Fracture
Red Blood Cell Count Decreased
Thrombocytopenia
Transaminases Increased
Transfusions 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 Transfusions 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!