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Aracytin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 18. View All

Aracytin FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 11

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

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6663727-7 | Enterococcal Infection, Enterococcal Sepsis
on Mar 24, 2010 Female patient from ITALY , 69 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). Patient experienced the following unwanted or unexpected effects: enterococcal infection, enterococcal sepsis. Aracytin dosage: 2400 Mg Total. During the same period patient was treated with ZAVEDOS (60 Mg Total) (View Zavedos Review and Zavedos Label ). Patient was hospitalized.

6662065-6 | Aphonia, Hyperpyrexia, Oropharyngitis Fungal, Pancreatitis Acute
Patient was taking Aracytin (View Usage). Patient had the following side effects: aphonia, hyperpyrexia, oropharyngitis fungal, pancreatitis acute on Mar 22, 2010 from ITALY Additional patient health information: Male patient , 68 years of age, was diagnosed with acute myeloid leukaemia and. Aracytin dosage: 300 Mg Total. During the same period patient was treated with ZAVEDOS (24 Mg X Day) (View Zavedos Review and Zavedos Label ), DEXRAZOXANE HYDROCHLORIDE (1000 Mg, Unk) (View Dexrazoxane Hydrochloride Review and Dexrazoxane Hydrochloride Label ). Patient was hospitalized.

6661533-0 | Abdominal Pain, Anaphylactoid Reaction, Bronchospasm, Diarrhoea, Hyperpyrexia, Stomatitis
Adverse event was reported on Mar 24, 2010 by a Male patient taking Aracytin (View Usage) (Dosage: 166 Mg X Day) was diagnosed with acute myeloid leukaemia, hyperpyrexia and. Location: ITALY , 33 years of age, After Aracytin was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), anaphylactoid reaction, bronchospasm, diarrhoea, hyperpyrexia, stomatitis. During the same period patient was treated with ZAVEDOS (17 Mg X Day) (View Zavedos Review and Zavedos Label ), AMPHOTERICINE B, LIPOSOME (1 Mg/m2, As Needed) (View Amphotericine B, Liposome Review and Amphotericine B, Liposome Label ).

6661532-9 | Oedema, Stomatitis, Stomatitis Necrotising, Vomiting
on Mar 24, 2010 Female patient from ITALY , 30 years of age, was diagnosed with acute monocytic leukaemia and was treated with Aracytin (View Usage). Patient experienced the following unwanted or unexpected effects: oedema, stomatitis, stomatitis necrotising, vomiting. Aracytin dosage: 300 Mg Total. During the same period patient was treated with ZAVEDOS (17 Mg, Daily) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (141 Mg, Daily) (View Etoposide Review and Etoposide Label ). Patient was hospitalized.


6657442-3 | Diarrhoea, Haemoptysis, Hepatic Failure, Mucosal Inflammation, Pleural Effusion, Pulmonary Mycosis
on Mar 19, 2010 Female patient from ITALY , 26 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). Patient had the following side effects: diarrhoea, haemoptysis, hepatic failure, mucosal inflammation, pleural effusion, pulmonary mycosis. Aracytin dosage: 28 G, Total. During the same period patient was treated with ZAVEDOS (64 Mg, Total) (View Zavedos Review and Zavedos Label ).

6646835-6 | Enterococcal Infection, Enterococcal Sepsis
Patient was taking Aracytin (View Usage). After Aracytin was administered, patient had the following side effects: enterococcal infection, enterococcal sepsis on Mar 11, 2010 from ITALY Additional patient health information: Female patient , 69 years of age, was diagnosed with acute myeloid leukaemia and. Aracytin dosage: 2400 Mg Total. During the same period patient was treated with ZAVEDOS (60 Mg Total) (View Zavedos Review and Zavedos Label ). Patient was hospitalized.

6646012-9 | Oedema, Stomatitis, Stomatitis Necrotising, Vomiting
Adverse event was reported on Mar 11, 2010 by a Female patient taking Aracytin (View Usage) (Dosage: 300 Mg Total) was diagnosed with acute monocytic leukaemia and. Location: ITALY , 30 years of age, Patient experienced the following unwanted or unexpected effects: oedema, stomatitis, stomatitis necrotising, vomiting. During the same period patient was treated with ZAVEDOS (17 Mg, Daily) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (141 Mg, Daily) (View Etoposide Review and Etoposide Label ). Patient was hospitalized.

6585665-0 | Oedema, Stomatitis, Stomatitis Necrotising, Vomiting
on Feb 05, 2010 Female patient from ITALY , 30 years of age, was diagnosed with acute monocytic leukaemia and was treated with Aracytin (View Usage). Patient had the following side effects: oedema, stomatitis, stomatitis necrotising, vomiting. Aracytin dosage: 300 Mg Total. During the same period patient was treated with ZAVEDOS (17 Mg, Daily) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (141 Mg, Daily) (View Etoposide Review and Etoposide Label ). Patient was hospitalized.

6585095-1 | Enterococcal Infection, Enterococcal Sepsis
on Feb 05, 2010 Female patient from ITALY , 69 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). After Aracytin was administered, patient had the following side effects: enterococcal infection, enterococcal sepsis. Aracytin dosage: 2400 Mg Total. During the same period patient was treated with ZAVEDOS (60 Mg Total) (View Zavedos Review and Zavedos Label ). Patient was hospitalized.

6582801-7 | Abdominal Pain, Anaphylactoid Reaction, Bronchospasm, Diarrhoea, Hyperpyrexia, Stomatitis
Patient was taking Aracytin (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), anaphylactoid reaction, bronchospasm, diarrhoea, hyperpyrexia, stomatitis on Feb 05, 2010 from ITALY Additional patient health information: Male patient , 33 years of age, was diagnosed with acute myeloid leukaemia, hyperpyrexia and. Aracytin dosage: 166 Mg X Day. During the same period patient was treated with ZAVEDOS (17 Mg X Day) (View Zavedos Review and Zavedos Label ), AMPHOTERICINE B, LIPOSOME (1 Mg/m2, As Needed) (View Amphotericine B, Liposome Review and Amphotericine B, Liposome Label ).

6582795-4 | Aphonia, Hyperpyrexia, Oropharyngitis Fungal, Pancreatitis Acute
Adverse event was reported on Feb 03, 2010 by a Male patient taking Aracytin (View Usage) (Dosage: 300 Mg, Total) was diagnosed with acute myeloid leukaemia and. Location: ITALY , 68 years of age, Patient had the following side effects: aphonia, hyperpyrexia, oropharyngitis fungal, pancreatitis acute. During the same period patient was treated with ZAVEDOS (24 Mg, Unk) (View Zavedos Review and Zavedos Label ), DEXRAZOXANE HYDROCHLORIDE (1000 Mg, Unk) (View Dexrazoxane Hydrochloride Review and Dexrazoxane Hydrochloride Label ). Patient was hospitalized.

6575489-2 | Diarrhoea, Haemoptysis, Hepatic Failure, Mucosal Inflammation, Pleural Effusion, Pulmonary Mycosis
on Jan 29, 2010 Female patient from ITALY , 26 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). After Aracytin was administered, patient had the following side effects: diarrhoea, haemoptysis, hepatic failure, mucosal inflammation, pleural effusion, pulmonary mycosis. Aracytin dosage: 28 G, Total. During the same period patient was treated with ZAVEDOS (64 Mg, Total) (View Zavedos Review and Zavedos Label ).

6573939-9 | Diarrhoea, Palatal Oedema
on Jan 27, 2010 Female patient from ITALY , 69 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, palatal oedema. Aracytin dosage: 340 Mg, X/day. During the same period patient was treated with ZAVEDOS (17 Mg, X/day) (View Zavedos Review and Zavedos Label ). Patient was hospitalized.

6573313-5 | Bronchopulmonary Aspergillosis, Enterococcal Sepsis, Human Herpesvirus 6 Infection, Pneumocystis Jiroveci Pneumonia
Patient was taking Aracytin (View Usage). Patient had the following side effects: bronchopulmonary aspergillosis, enterococcal sepsis, human herpesvirus 6 infection, pneumocystis jiroveci pneumonia on Jan 27, 2010 from ITALY Additional patient health information: Male patient , 59 years of age, was diagnosed with acute myeloid leukaemia and. Aracytin dosage: 400 Mg, X/day. During the same period patient was treated with ZAVEDOS (25 Mg, X/day) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (200 Mg, X/day) (View Etoposide Review and Etoposide Label ).

6573301-9 | Hyperpyrexia, Pneumonia Bacterial, Staphylococcal Sepsis
Adverse event was reported on Jan 27, 2010 by a Female patient taking Aracytin (View Usage) (Dosage: 266 Mg, X/day) was diagnosed with acute myeloid leukaemia and. Location: ITALY , 67 years of age, After Aracytin was administered, patient had the following side effects: hyperpyrexia, pneumonia bacterial, staphylococcal sepsis. During the same period patient was treated with ZAVEDOS (18 Mg, X/day) (View Zavedos Review and Zavedos Label ). Patient was hospitalized.

6571967-0 | Herpes Virus Infection, Hyperpyrexia, Pseudomonas Infection, Respiratory Failure, Staphylococcal Sepsis
on Jan 26, 2010 Male patient from ITALY , 50 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). Patient experienced the following unwanted or unexpected effects: herpes virus infection, hyperpyrexia, pseudomonas infection, respiratory failure, staphylococcal sepsis. Aracytin dosage: 418 Mg, 1x/day. During the same period patient was treated with ZAVEDOS (25 Mg, 1x/day) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (209 Mg, 1x/day) (View Etoposide Review and Etoposide Label ).

6570271-4 | Diarrhoea, Gastrointestinal Inflammation, Hyperpyrexia, Pleural Effusion
on Jan 26, 2010 Male patient from ITALY , 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with Aracytin (View Usage). Patient had the following side effects: diarrhoea, gastrointestinal inflammation, hyperpyrexia, pleural effusion. Aracytin dosage: 360 Mg, X/day. During the same period patient was treated with ZAVEDOS (22 Mg, X/day) (View Zavedos Review and Zavedos Label ), ETOPOSIDE (180 Mg, X/day) (View Etoposide Review and Etoposide Label ). Patient was hospitalized.

6570267-2 | Enterobacter Sepsis, Hyperpyrexia, Pneumonia
Patient was taking Aracytin (View Usage). After Aracytin was administered, patient had the following side effects: enterobacter sepsis, hyperpyrexia, pneumonia (What is pneumonia?) on Jan 26, 2010 from ITALY Additional patient health information: Male patient , 65 years of age, was diagnosed with acute myeloid leukaemia and. Aracytin dosage: 16 G, Total. During the same period patient was treated with ZAVEDOS (64 Mg Total) (View Zavedos Review and Zavedos Label ).


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Aracytin Questions, Answers, Feedback and Comments

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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 Aracytin 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 Aracytin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Aracytin 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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Aracytin Reactions
Abdominal PainWhat is Abdominal pain?
Anaphylactoid Reaction
Aphonia
Bronchopulmonary Aspergillosis
Bronchospasm
Diarrhoea
Enterobacter Sepsis
Enterococcal Infection
Enterococcal Sepsis
Gastrointestinal Inflammation
Haemoptysis
Hepatic Failure
Herpes Virus Infection
Human Herpesvirus 6 Infection
Hyperpyrexia
Mucosal Inflammation
Oedema
Oropharyngitis Fungal
Palatal Oedema
Pancreatitis Acute
Pleural Effusion
Pneumocystis Jiroveci Pneumonia
PneumoniaWhat is Pneumonia?
Pneumonia Bacterial
Pseudomonas Infection
Pulmonary Mycosis
Staphylococcal Sepsis
Stomatitis
Stomatitis Necrotising
Vomiting
Aracytin 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 Aracytin 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!