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Igivnex adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Igivnex FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 3

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

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6887730-7 | Dermatitis Exfoliative
on Jul 08, 2010 Male patient from CANADA , 58 years of age, was diagnosed with neurological symptom and was treated with Igivnex (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis exfoliative. Igivnex dosage: ; Iv.

6761696-2 | Agitation, Alopecia, Body Temperature Increased, Chills, Livedo Reticularis, Pruritus, Rash
Patient was taking Igivnex (View Usage). Patient had the following side effects: agitation, alopecia, body temperature increased, chills, livedo reticularis, pruritus, rash (What is rash?) on Apr 26, 2010 from UNITED KINGDOM Additional patient health information: Male patient , child 5 years of age, weighting 46.63 lb, . Igivnex dosage: 42.3 Gm; Total; Iv. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), CHLORAL HYDRATE (View Chloral Hydrate Review and Chloral Hydrate Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).

6761690-1 | Chills, Dyspnoea, Fluid Overload, Hypertension, Hypoxia, Nausea, Pulmonary Oedema, Pyrexia, Tachycardia
Adverse event was reported on Apr 23, 2010 by a Male patient taking Igivnex (View Usage) (Dosage: 500 Ml; Total; Iv) . Location: CANADA , 71 years of age, After Igivnex was administered, patient had the following side effects: chills, dyspnoea, fluid overload, hypertension, hypoxia, nausea (What is nausea?), pulmonary oedema, pyrexia, tachycardia.

6653882-7 | Chills, Dyspnoea, Fluid Overload, Hypertension, Hypoxia, Nausea, Oxygen Saturation Decreased, Pulmonary Oedema, Pyrexia
on Mar 05, 2010 Male patient from CANADA , 71 years of age, was treated with Igivnex (View Usage). Patient experienced the following unwanted or unexpected effects: chills, dyspnoea, fluid overload, hypertension, hypoxia, nausea (What is nausea?), oxygen saturation decreased, pulmonary oedema, pyrexia. Igivnex dosage: 500 Ml;total;iv.


6607643-5 | Anaemia Haemolytic Autoimmune, Blood Bilirubin Decreased, Blood Lactate Dehydrogenase Increased, Blood Pressure Systolic Increased, Dyspnoea Paroxysmal Nocturnal, Haemoglobinuria, Heart Rate Decreased, Platelet Count Decreased, White Blood Cell Count Decreased
on Feb 01, 2010 Male patient from CANADA , 77 years of age, weighting 155.1 lb, was diagnosed with chronic inflammatory demyelinating polyradiculoneuropathy and was treated with Igivnex (View Usage). Patient had the following side effects: anaemia haemolytic autoimmune, blood bilirubin decreased, blood lactate dehydrogenase increased, blood pressure systolic increased, dyspnoea paroxysmal nocturnal, haemoglobinuria, heart rate decreased, platelet count decreased, white blood cell count decreased. Igivnex dosage: 70 Gm; Total; Iv, 100 Gm; Total; Iv. During the same period patient was treated with GAMUNEX (70 Gm; Qd; Iv, 10 Gm; Qd; Iv) (View Gamunex Review and Gamunex Label ). Patient was hospitalized.

6574130-2 | Anaemia Haemolytic Autoimmune, Blood Pressure Systolic Increased, Condition Aggravated, Dyspnoea, Dyspnoea Paroxysmal Nocturnal, Haemoglobinuria, Platelet Count Decreased, Polychromasia, Punctate Basophilia
Patient was taking Igivnex (View Usage). After Igivnex was administered, patient had the following side effects: anaemia haemolytic autoimmune, blood pressure systolic increased, condition aggravated, dyspnoea, dyspnoea paroxysmal nocturnal, haemoglobinuria, platelet count decreased, polychromasia, punctate basophilia on Jan 04, 2010 from CANADA Additional patient health information: Male patient , 77 years of age, weighting 155.1 lb, was diagnosed with chronic inflammatory demyelinating polyradiculoneuropathy and. Igivnex dosage: 70 Gm; Total; Iv. During the same period patient was treated with GAMUNEX (70 Gm;qd; Iv) (View Gamunex Review and Gamunex Label ). Patient was hospitalized.

6501993-9 | Acute Respiratory Distress Syndrome, Device Related Infection, Enterococcal Infection, Fluid Overload, Pulmonary Hypertension, Respiratory Failure
Adverse event was reported on Nov 24, 2009 by a Male patient taking Igivnex (View Usage) (Dosage: Qd;iv) was diagnosed with polymyositis and. Location: CANADA , 65 years of age, Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, device related infection, enterococcal infection, fluid overload, pulmonary hypertension (What is pulmonary hypertension?), respiratory failure.

6435569-9 | Hypersensitivity, Infusion Related Reaction
on Feb 22, 2008 Female patient from CANADA , 30 years of age, was treated with Igivnex (View Usage). Patient had the following side effects: hypersensitivity, infusion related reaction. Igivnex dosage: .

6369201-X | Cerebral Infarction, Confusional State, Quadriplegia, Stupor
on Aug 28, 2009 Female patient from MEXICO , 68 years of age, was diagnosed with guillain-barre syndrome (What is guillain-barre syndrome?) and was treated with Igivnex (View Usage). After Igivnex was administered, patient had the following side effects: cerebral infarction, confusional state, quadriplegia, stupor. Igivnex dosage: 5 G, 5 G Daily For 4 Days Intravenous (not Otherwise Specified).

5193665-0 | Blood Culture Positive, Blood Urine Present, Body Temperature Increased, Candidiasis, Cough, Culture Urine Positive, Depressed Level Of Consciousness, Fungal Infection, Pneumonia
Patient was taking Igivnex (View Usage). Patient experienced the following unwanted or unexpected effects: blood culture positive, blood urine present, body temperature increased, candidiasis, cough, culture urine positive, depressed level of consciousness, fungal infection (What is fungal infection?), pneumonia (What is pneumonia?) on Dec 06, 2006 from CANADA Additional patient health information: Male patient , 77 years of age, was diagnosed with idiopathic thrombocytopenic purpura and. Igivnex dosage: . During the same period patient was treated with GAMUNEX (View Gamunex Review and Gamunex Label ), PLATELET TRANSFUSION (THROMBAPHORESIS) (PLATELETS, HUMAN BLOOD) (View Platelet Transfusion (thrombaphoresis) (platelets, Human Blood) Review and Platelet Transfusion (thrombaphoresis) (platelets, Human Blood) 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 Igivnex 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 Igivnex quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Igivnex 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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During the same period patient was treated with IGIVNEX (Iv ; 20 Gm; Iv) (View Igivnex Review and Igivnex Label ). 6924394-8 | Treponema Test Positive

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igivnex Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: imatinib Episodes: 6: Diagnosed with major depression.Side ...

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Igivnex Reactions
Acute Respiratory Distress Syndrome
Agitation
Alopecia
Anaemia Haemolytic Autoimmune
Blood Bilirubin Decreased
Blood Culture Positive
Blood Lactate Dehydrogenase Increased
Blood Pressure Systolic Increased
Blood Urine Present
Body Temperature Increased
Candidiasis
Cerebral Infarction
Chills
Condition Aggravated
Confusional State
Cough
Culture Urine Positive
Depressed Level Of Consciousness
Dermatitis Exfoliative
Device Related Infection
Dyspnoea
Dyspnoea Paroxysmal Nocturnal
Fluid Overload
Haemoglobinuria
Hypertension
Hypoxia
NauseaWhat is Nausea?
Platelet Count Decreased
Pulmonary Oedema
Pyrexia
Igivnex 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 Igivnex 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!