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Anakinra adverse events reported to FDA.

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Summary

FDA Adverse Reports: 13. View All

Anakinra FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 10

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

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7009199-4 | Lung Disorder, Lymphadenopathy, Renal Impairment
on Sep 08, 2010 Female patient from UNITED STATES , child 11 years of age, was diagnosed with juvenile arthritis and was treated with Anakinra (View Usage). Patient experienced the following unwanted or unexpected effects: lung disorder, lymphadenopathy, renal impairment. Anakinra dosage: (subcutaneous). During the same period patient was treated with SOLU MEDROL ((pulses Intravenous (not Otherwise Specified))) (View Solu-medrol Review and Solu-medrol Label ), CYCLOSPORINE ((oral)) (View Cyclosporine Review and Cyclosporine Label ), METHOTREXATE ((subcutaneous)) (View Methotrexate Review and Methotrexate Label ), LEFLUNOMIDE ((oral)) (View Leflunomide Review and Leflunomide Label ), SULINDAC ((oral)) (View Sulindac Review and Sulindac Label ).

6994623-3 | Dyspepsia, Furuncle
Patient was taking Anakinra (View Usage). Patient had the following side effects: dyspepsia, furuncle on Sep 15, 2010 from UNITED STATES Additional patient health information: Male patient , 60 years of age, . Anakinra dosage: 100 Mg Every Day Sq.

6761522-1 | Acute Coronary Syndrome, Injection Site Pain
Adverse event was reported on May 20, 2010 by a Female patient taking Anakinra (View Usage) (Dosage: 100 Mg Qd Subcutaneous) was diagnosed with acute myocardial infarction and. Location: UNITED STATES , 34 years of age, After Anakinra was administered, patient had the following side effects: acute coronary syndrome, injection site pain.

6430754-4 | Gastrointestinal Necrosis, Sepsis, Upper Gastrointestinal Haemorrhage
on Nov 05, 2009 Male patient from UNITED STATES , 65 years of age, weighting 205.9 lb, was diagnosed with gout (What is gout?) and was treated with Anakinra (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal necrosis, sepsis (What is sepsis?), upper gastrointestinal haemorrhage. Anakinra dosage: 2 Doses. Patient was hospitalized.


4556001-6 | Acute Respiratory Distress Syndrome, Pneumonia
on Jun 16, 2004 Female patient from , 59 years of age, weighting 108.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Anakinra (View Usage). Patient had the following side effects: acute respiratory distress syndrome, pneumonia (What is pneumonia?). Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ESTROGENS CONJUGATED (View Estrogens Conjugated Review and Estrogens Conjugated Label ), CELECOXIB (View Celecoxib Review and Celecoxib Label ), PAROXETINE HYDROCHLORIDE (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

4555997-6 | Pneumonia
Patient was taking Anakinra (View Usage). After Anakinra was administered, patient had the following side effects: pneumonia (What is pneumonia?) on Jun 16, 2004 from Additional patient health information: Female patient , 60 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ). Patient was hospitalized.

4555993-9 | Pneumonia
Adverse event was reported on Jun 16, 2004 by a Male patient taking Anakinra (View Usage) (Dosage: Daily, Sc) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: , 78 years of age, Patient experienced the following unwanted or unexpected effects: pneumonia (What is pneumonia?). During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

4555991-5 | Pneumonia
on Jun 16, 2004 Male patient from , 77 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Anakinra (View Usage). Patient had the following side effects: pneumonia (What is pneumonia?). Anakinra dosage: Sc. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), CELECOXIB (View Celecoxib Review and Celecoxib Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ). Patient was hospitalized.

4555983-6 | Pneumonia
on Jun 16, 2004 Female patient from , 33 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Anakinra (View Usage). After Anakinra was administered, patient had the following side effects: pneumonia (What is pneumonia?). Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with METHOTREXATE (7.5 Mg, Weekly, Po) (View Methotrexate Review and Methotrexate Label ), PREDNISONE (10 Mg, Daily, Po) (View Prednisone Review and Prednisone Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ), AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE (View Amlodipine And Benazepril Hydrochloride Review and Amlodipine And Benazepril Hydrochloride Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), BECLOMETHASONE DIPROPIONATE (View Beclomethasone Dipropionate Review and Beclomethasone Dipropionate Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ). Patient was hospitalized.

4555979-4 | Pneumonia
Patient was taking Anakinra (View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (What is pneumonia?) on Jun 16, 2004 from Additional patient health information: Female patient , 70 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with LEVOTHRYROXINE SODIUM (View Levothryroxine Sodium Review and Levothryroxine Sodium Label ), PAROXETINE HYDROCHLORIDE (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), BUDESONIDE (View Budesonide Review and Budesonide Label ), ALBUTEROL SULFATE (View Albuterol Sulfate Review and Albuterol Sulfate Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ). Patient was hospitalized.

4555975-7 | Pneumonia
Adverse event was reported on Jun 16, 2004 by a Female patient taking Anakinra (View Usage) (Dosage: 100 Mg, Daily, Sc) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: , 82 years of age, Patient had the following side effects: pneumonia (What is pneumonia?). During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), NICOTINIC ACID (View Nicotinic Acid Review and Nicotinic Acid Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), PAROXETINE HYDROCHLORIDE (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

4555972-1 | Pneumonia
on Jun 16, 2004 Male patient from , 55 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Anakinra (View Usage). After Anakinra was administered, patient had the following side effects: pneumonia (What is pneumonia?). Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), MYLANTA (View Mylanta Review and Mylanta Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ). Patient was hospitalized.

4555970-8 | Cellulitis
on Jun 16, 2004 Female patient from , 50 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Anakinra (View Usage). Patient experienced the following unwanted or unexpected effects: cellulitis (What is cellulitis?). Anakinra dosage: 100 Mg, Daily, Sc. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), TRAZODONE HCL (View Trazodone Hcl Review and Trazodone Hcl Label ), CALCIUM POLYCARBOPHIL (View Calcium Polycarbophil Review and Calcium Polycarbophil Label ), SERTRALINE HYDROCHLORIDE (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ), BUMETANIDE (View Bumetanide Review and Bumetanide Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen 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 Anakinra 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 Anakinra quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Anakinra 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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Anakinra Reactions
Acute Coronary Syndrome
Acute Respiratory Distress Syndrome
CellulitisWhat is Cellulitis?
Dyspepsia
Furuncle
Gastrointestinal Necrosis
Injection Site Pain
Lung Disorder
Lymphadenopathy
PneumoniaWhat is Pneumonia?
Renal Impairment
SepsisWhat is Sepsis?
Upper Gastrointestinal Haemorrhage
Anakinra 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 Anakinra 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!