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Sendoxan adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Sendoxan FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 4

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

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5781727-6 | Fatigue, Pyrexia
on May 22, 2008 Male patient from UNITED STATES , 71 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with Sendoxan (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, pyrexia. Sendoxan dosage: . During the same period patient was treated with DOXORUBICIN HCL (1 Dosage Form = 2mg/ml Inj.) (View Doxorubicin Hcl Review and Doxorubicin Hcl Label ), DELTISON (View Deltison Review and Deltison Label ), ONCOVIN (1 Dosage Form = 1mg/ml.) (View Oncovin Review and Oncovin Label ), CARBAMAZEPINE (View Carbamazepine Review and Carbamazepine Label ), ACYCLOVIR (View Acyclovir Review and Acyclovir Label ). Patient was hospitalized.

5352200-4 | Progressive Multifocal Leukoencephalopathy
Patient was taking Sendoxan (View Usage). Patient had the following side effects: progressive multifocal leukoencephalopathy on Jun 08, 2007 from FINLAND Additional patient health information: Female patient , 72 years of age, was diagnosed with burkitt's lymphoma and. Sendoxan dosage: . During the same period patient was treated with TREXAN (ORION) (View Trexan (orion) Review and Trexan (orion) Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), MABTHERA (View Mabthera Review and Mabthera Label ), ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), ONCOVIN (View Oncovin Review and Oncovin Label ), CYTARABINE (View Cytarabine Review and Cytarabine Label ). Patient was hospitalized and became disabled.

5349713-8 | Progressive Multifocal Leukoencephalopathy
Adverse event was reported on May 31, 2007 by a Female patient taking Sendoxan (View Usage) (Dosage: ) was diagnosed with burkitt's lymphoma and. Location: UNITED STATES , 72 years of age, After Sendoxan was administered, patient had the following side effects: progressive multifocal leukoencephalopathy. During the same period patient was treated with TREXAN (ORION) (View Trexan (orion) Review and Trexan (orion) Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), MABTHERA (View Mabthera Review and Mabthera Label ), ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), ONCOVIN (View Oncovin Review and Oncovin Label ), CYTARABINE (View Cytarabine Review and Cytarabine Label ). Patient was hospitalized and became disabled.

5349643-1 | Jc Virus Infection, Progressive Multifocal Leukoencephalopathy
on May 31, 2007 Male patient from UNITED STATES , 63 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with Sendoxan (View Usage). Patient experienced the following unwanted or unexpected effects: jc virus infection, progressive multifocal leukoencephalopathy. Sendoxan dosage: . During the same period patient was treated with RITUXIMAB (View Rituximab Review and Rituximab Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), ONCOVIN (View Oncovin Review and Oncovin Label ), CYTARABINE (View Cytarabine Review and Cytarabine Label ), ORAMET (View Oramet Review and Oramet Label ), EFFEXOR (View Effexor Review and Effexor Label ), DEPRAKINE DEPOT (View Deprakine Depot Review and Deprakine Depot Label ).


5334383-5 | Blood Pressure Decreased, Heart Rate Decreased, Hepatic Failure, Multi-organ Failure, Renal Failure
on May 04, 2007 Male patient from UNITED STATES , 44 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and was treated with Sendoxan (View Usage). Patient had the following side effects: blood pressure decreased, heart rate decreased, hepatic failure, multi-organ failure, renal failure. Sendoxan dosage: . During the same period patient was treated with DEXAMETHASONE 0.5MG TAB (View Dexamethasone 0.5mg Tab Review and Dexamethasone 0.5mg Tab Label ).

5008256-1 | Bone Disorder, Breath Odour, Dysgeusia, Impaired Healing, Oral Pain, Osteonecrosis, Tooth Disorder, Tooth Extraction
Patient was taking Sendoxan (View Usage). After Sendoxan was administered, patient had the following side effects: bone disorder, breath odour, dysgeusia, impaired healing, oral pain, osteonecrosis (What is osteonecrosis?), tooth disorder (What is tooth disorder?), tooth extraction on May 11, 2006 from NORWAY Additional patient health information: Male patient , 59 years of age, was diagnosed with hypercalcaemia and. Sendoxan dosage: 400 Mg, Qw. During the same period patient was treated with PREDNISOLONE (15 Daily) (View Prednisolone Review and Prednisolone Label ), VELCADE (4 Doses Over 4 Weeks) (View Velcade Review and Velcade Label ), ZOMETA (4 Mg, Qmo) (View Zometa Review and Zometa Label ).

5005696-1 | Bone Disorder, Breath Odour, Dysgeusia, Impaired Healing, Oral Pain, Tooth Disorder, Tooth Extraction
Adverse event was reported on May 11, 2006 by a Male patient taking Sendoxan (View Usage) (Dosage: 400 Mg, Qw) was diagnosed with hypercalcaemia and. Location: NORWAY , 59 years of age, Patient experienced the following unwanted or unexpected effects: bone disorder, breath odour, dysgeusia, impaired healing, oral pain, tooth disorder (What is tooth disorder?), tooth extraction. During the same period patient was treated with PREDNISOLONE (15 Daily) (View Prednisolone Review and Prednisolone Label ), VELCADE (4 Doses Over 4 Weeks) (View Velcade Review and Velcade Label ), ZOMETA (4 Mg, Qmo) (View Zometa Review and Zometa Label ).

4635106-5 | Agranulocytosis, Hepatic Enzyme Increased, Hepatitis B, Lung Disorder, Pleurisy, Pneumonia, Respiratory Tract Infection
on Apr 04, 2005 Female patient from , 65 years of age, was diagnosed with vasculitis (What is vasculitis?), polyneuropathy and was treated with Sendoxan (View Usage). Patient had the following side effects: agranulocytosis, hepatic enzyme increased, hepatitis b (What is hepatitis b?), lung disorder, pleurisy, pneumonia (What is pneumonia?), respiratory tract infection. Sendoxan dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), IMUREL (View Imurel Review and Imurel 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 Sendoxan 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 Sendoxan quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Sendoxan 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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Sendoxan Reactions
Agranulocytosis
Blood Pressure Decreased
Bone Disorder
Breath Odour
Dysgeusia
Fatigue
Heart Rate Decreased
Hepatic Enzyme Increased
Hepatic Failure
Hepatitis BWhat is Hepatitis b?
Impaired Healing
Jc Virus Infection
Lung Disorder
Multi-organ Failure
Oral Pain
OsteonecrosisWhat is Osteonecrosis?
Pleurisy
PneumoniaWhat is Pneumonia?
Progressive Multifocal Leukoencephalopathy
Pyrexia
Renal Failure
Respiratory Tract Infection
Tooth DisorderWhat is Tooth disorder?
Tooth Extraction
Sendoxan 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 Sendoxan 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!