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I was given 3 vials of Remicade last February 18, 2010 as treatment ...Keep Reading

I also recieved Remicade for my Ulcerative Colitis and after that I developed Alopecia ...Keep Reading

I have been on Remicade since last December 2009 ... it ...Keep Reading

Have been on Orencia several mo,s and developed lower leg edema 3+ and ...Keep Reading

Treated with Remicade for Ulcerative Colitis. Almost immediately developed Narcolepsy. Treatment discontinued,...Keep Reading

Wondering if there is an possibility that the 2 tooth abcesses I've had in ...Keep Reading

I am experiencing hair loss. I have had 4 remicade infusions ...Keep Reading

i have been diagnosed with crohn's disease since 1990. i have used many ...Keep Reading

I noticed that after my third Remicade treatment that my mood changed. I ...Keep Reading

I took remicade for five months for my RA and started with a very ...Keep Reading

I have been having kidney trouble, glomerulonephritis to be specific, it was ...Keep Reading

Same here, did your hair come back after stopping Remicade? andrealightfoot@msn.com...Keep Reading

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Indicate Your Remicade Side Effects
Depression (5)
Tooth Decay (4)
Mouth Sores (3)
Rash (3)
Cranial Nerve Palsy (2)
Hair Loss (2)
Nausea Amd Dizziness Flush Face (2)
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Common Remicade Side Effects

top 5 Remicade|Depression|Tooth deca|Mouth sore|Rash|Cranial ne|Hair loss|Nausea amd adverse effects>>See All Remicade Side Effects

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Remicade adverse events reported to FDA.

Have You Experienced unusual Remicade symptoms? PatientsVille.com collects and analyzes Remicade side effect and adverse reports submitted by Remicade users, such as Fatigue, diarrhea, nausea, joint pain, sore throat|eyeritis |atrial fibrillation |Invasive vaginal fungal infection, athletes foot, all|Flusing feeling in head, tightness in chest,|.

Summary

FDA Adverse Reports: 23439. View All

Remicade FDA safety alerts: 2001 2004 2008 2009

Reported deaths: 2435

Reported hospitalizations: 11005

More About Remicade

Post Your Unusual Symptoms:

Most Reported
1Depression
2Tooth Decay
3Chest Discomfort
4Rash
5Cranial Nerve Palsy
6Lung Infiltration
7Mouth Sores
8Tachycardia
9Tired
10Hair Loss
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Recent Drug Reports

Fatigue, diarrhea, nausea, joint pain, sore throat

eyeritis

atrial fibrillation

Invasive vaginal fungal infection, athletes foot, all

Flusing feeling in head, tightness in chest,

More Remicade Side Effect Reports

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

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Showing 1-50 of 23439  Next Page  >

7023159-9 | Pyrexia
on Sep 20, 2010 Female patient from UNITED STATES , child 8 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: pyrexia. Remicade dosage: .

7022893-4 | Neoplasm Malignant
Patient was taking Remicade (View Usage). Patient had the following side effects: neoplasm malignant on Sep 20, 2010 from CANADA Additional patient health information: Male patient , weighting 231.9 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: . During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ), ISONIAZID (View Isoniazid Review and Isoniazid Label ), PYRAZINAMIDE (View Pyrazinamide Review and Pyrazinamide Label ).

7022892-2 | Intestinal Resection
Adverse event was reported on Sep 20, 2010 by a Male patient taking Remicade (View Usage) (Dosage: Q7 Times 52) . Location: CANADA , weighting 180.8 lb, After Remicade was administered, patient had the following side effects: intestinal resection. During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), SOLU CORTEF (View Solu-cortef Review and Solu-cortef Label ).

7022891-0 | Peripheral Nerve Injury, Skin Laceration
on Sep 20, 2010 Male patient from CANADA , weighting 187.4 lb, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: peripheral nerve injury, skin laceration. Remicade dosage: Loading Doses. Patient was hospitalized.


7022890-9 | Pancreatitis
on Sep 20, 2010 Female patient from CANADA , weighting 123.5 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: pancreatitis. Remicade dosage: . During the same period patient was treated with IMURAN (View Imuran Review and Imuran Label ). Patient was hospitalized.

7022889-2 | Fall, Wrist Fracture
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: fall (What is fall?), wrist fracture on Sep 20, 2010 from CANADA Additional patient health information: Female patient , weighting 204.5 lb, was diagnosed with psoriasis and. Remicade dosage: . During the same period patient was treated with ATARAX (View Atarax Review and Atarax Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), CODEINE (View Codeine Review and Codeine Label ), TYLENOL (View Tylenol Review and Tylenol Label ), IMOVANE (View Imovane Review and Imovane Label ), REACTINE (View Reactine Review and Reactine Label ), FLONASE (View Flonase Review and Flonase Label ). Patient was hospitalized.

7022260-3 | Arthralgia, Blood Pressure Decreased, Dyspnoea, Erythema, Infusion Related Reaction, Joint Stiffness, Myalgia, Nausea, Oropharyngeal Pain
Adverse event was reported on Sep 20, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with psoriasis, osteopenia, blood cholesterol, gastrooesophageal reflux disease, depression (What is depression?) and. Location: UNITED STATES , weighting 145.0 lb, Patient experienced the following unwanted or unexpected effects: arthralgia, blood pressure decreased, dyspnoea, erythema, infusion related reaction, joint stiffness, myalgia, nausea (What is nausea?), oropharyngeal pain. During the same period patient was treated with PREMARIAN CREAM (View Premarian Cream Review and Premarian Cream Label ), ACTONEL (View Actonel Review and Actonel Label ), ZETIA (View Zetia Review and Zetia Label ), NEXIUM (View Nexium Review and Nexium Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), CHANTIX (View Chantix Review and Chantix Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

7022125-7 | Malignant Melanoma
on Sep 20, 2010 Female patient from CANADA , weighting 218.3 lb, was diagnosed with psoriasis and was treated with Remicade (View Usage). Patient had the following side effects: malignant melanoma. Remicade dosage: .

7022119-1 | Fatigue, Headache, Influenza Like Illness, Oropharyngeal Pain, Pyrexia, Vomiting
on Sep 21, 2010 Female patient from FRANCE , 39 years of age, weighting 123.5 lb, was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: fatigue, headache (What is headache?), influenza like illness, oropharyngeal pain, pyrexia, vomiting. Remicade dosage: .

7022118-X | Hypersensitivity, Myoclonus
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity, myoclonus on Sep 20, 2010 from JAPAN Additional patient health information: Female patient , 57 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: 4th Dose. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

7021982-8 | Pyoderma Gangrenosum
Adverse event was reported on Sep 20, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) . Location: GERMANY , 44 years of age, Patient had the following side effects: pyoderma gangrenosum.

7021921-X | Anal Abscess, Infusion Related Reaction
on Sep 19, 2010 Male patient from CHINA , 15 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: anal abscess, infusion related reaction. Remicade dosage: .

7021915-4 | Arterial Insufficiency, Arterial Thrombosis Limb, Myocardial Infarction
on Sep 15, 2010 Male patient from CANADA , 60 years of age, weighting 212.7 lb, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?), dry eye, angina pectoris, seasonal allergy and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: arterial insufficiency, arterial thrombosis limb, myocardial infarction. Remicade dosage: . During the same period patient was treated with FLURAZEPAM (View Flurazepam Review and Flurazepam Label ), AMITRIPTYLINE (View Amitriptyline Review and Amitriptyline Label ), TEARS NATURALE (View Tears Naturale Review and Tears Naturale Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), CLARITIN (View Claritin Review and Claritin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

7021914-2 | Erythema, Hypoaesthesia Oral, Infusion Related Reaction, Lip Swelling
Patient was taking Remicade (View Usage). Patient had the following side effects: erythema, hypoaesthesia oral, infusion related reaction, lip swelling on Sep 20, 2010 from CANADA Additional patient health information: Female patient , weighting 124.1 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: . During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ).

7021899-9 | Chills, Cough, Suffocation Feeling
Adverse event was reported on Sep 19, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with juvenile arthritis and. Location: ISRAEL , 20 years of age, After Remicade was administered, patient had the following side effects: chills, cough, suffocation feeling.

7020883-9 | Prostate Cancer
on Sep 16, 2010 Male patient from UNITED STATES , weighting 213.2 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: prostate cancer (What is prostate cancer?). Remicade dosage: .

7020671-3 | Subcutaneous Abscess
on Sep 17, 2010 Female patient from UNITED STATES , weighting 136.2 lb, was diagnosed with inflammatory bowel disease, irritable bowel syndrome (What is irritable bowel syndrome?) and was treated with Remicade (View Usage). Patient had the following side effects: subcutaneous abscess. Remicade dosage: . During the same period patient was treated with ANTIBIOTIC (View Antibiotic Review and Antibiotic Label ), HYDROCODONE BITARTRATE AND ACETAMINOPHEN (View Hydrocodone Bitartrate And Acetaminophen Review and Hydrocodone Bitartrate And Acetaminophen Label ). Patient was hospitalized.

7020463-5 | Gingival Bleeding, Hepatic Steatosis, Hepatitis Alcoholic, Urticaria
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: gingival bleeding, hepatic steatosis, hepatitis alcoholic, urticaria on Sep 20, 2010 from BRAZIL Additional patient health information: Male patient , 65 years of age, weighting 158.7 lb, was diagnosed with psoriasis and. Remicade dosage: .

7020282-X | Dyspnoea, Nausea
Adverse event was reported on Sep 18, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with colitis ulcerative and. Location: ITALY , child 8 years of age, Patient experienced the following unwanted or unexpected effects: dyspnoea, nausea (What is nausea?).

7020029-7 | Confusional State, Cyanosis, Dizziness, Dyspnoea, Feeling Hot, Flushing, Infusion Related Reaction, Swollen Tongue
on Sep 17, 2010 Female patient from DENMARK , 29 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: confusional state, cyanosis, dizziness (What is dizziness?), dyspnoea, feeling hot, flushing, infusion related reaction, swollen tongue. Remicade dosage: 18th Infusion. During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ).

7020028-5 | Enteritis, Hypersensitivity, Therapeutic Response Decreased, Tuberculous Pleurisy
on Sep 17, 2010 Female patient from JAPAN , weighting 88.18 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), prophylaxis, hypertension and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: enteritis, hypersensitivity, therapeutic response decreased, tuberculous pleurisy. Remicade dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), OMEPRAL (View Omepral Review and Omepral Label ), AMLODIPINE BESILATE (View Amlodipine Besilate Review and Amlodipine Besilate Label ), ACTONEL (View Actonel Review and Actonel Label ). Patient was hospitalized.

7019991-8 | Abdominal Discomfort, Anaemia, Arthralgia, Hypotension, Incoherent, Leukocytosis, Oedema, Somnolence
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, anaemia, arthralgia, hypotension, incoherent, leukocytosis, oedema, somnolence on Sep 16, 2010 from COLOMBIA Additional patient health information: Female patient , 68 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and. Remicade dosage: . During the same period patient was treated with THYROXIN (View Thyroxin Review and Thyroxin Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), PLASIL (View Plasil Review and Plasil Label ), TRAMADOL (View Tramadol Review and Tramadol Label ). Patient was hospitalized.

7019988-8 | Abdominal Discomfort, Anaemia, Arthralgia, Hypotension, Incoherent, Leukocytosis, Oedema, Somnolence
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and. Location: PERU , 68 years of age, Patient had the following side effects: abdominal discomfort, anaemia, arthralgia, hypotension, incoherent, leukocytosis, oedema, somnolence. During the same period patient was treated with THYROXIN (View Thyroxin Review and Thyroxin Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), PLASIL (View Plasil Review and Plasil Label ), TRAMADOL (View Tramadol Review and Tramadol Label ). Patient was hospitalized.

7019987-6 | Hypoaesthesia Oral, Infusion Related Reaction, Lip Swelling, Rash, Swelling Face
on Sep 17, 2010 Male patient from CANADA , weighting 185.2 lb, was diagnosed with colitis ulcerative and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: hypoaesthesia oral, infusion related reaction, lip swelling, rash (What is rash?), swelling face. Remicade dosage: .

7019986-4 | Hospitalisation
on Sep 17, 2010 Female patient from CANADA , weighting 132.3 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: hospitalisation. Remicade dosage: A Total Of 52 Weeks. During the same period patient was treated with SOLU CORTEF (View Solu-cortef Review and Solu-cortef Label ). Patient was hospitalized.

7019914-1 | Arthralgia, Cartilage Injury, Fatigue, Foot Operation, Groin Pain, Influenza Like Illness, Intervertebral Disc Protrusion, Thyroid Disorder
Patient was taking Remicade (View Usage). Patient had the following side effects: arthralgia, cartilage injury, fatigue, foot operation, groin pain, influenza like illness, intervertebral disc protrusion, thyroid disorder on Sep 17, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 120.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), injury, convulsion, gastric disorder, dizziness (What is dizziness?), osteoporosis (What is osteoporosis?) and. Remicade dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BENTYL (View Bentyl Review and Bentyl Label ), MECLIZINE (View Meclizine Review and Meclizine Label ), BONIVA (View Boniva Review and Boniva Label ).

7019913-X | Colitis Ulcerative, Decreased Appetite, Weight Decreased
Adverse event was reported on Sep 17, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) was diagnosed with colitis ulcerative, blood cholesterol abnormal, hypertension and. Location: UNITED STATES , weighting 142.0 lb, After Remicade was administered, patient had the following side effects: colitis ulcerative, decreased appetite, weight decreased. During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

7019912-8 | Dyspnoea, Infusion Related Reaction, Malaise, Myalgia, Pyrexia, Therapeutic Response Decreased
on Sep 17, 2010 Female patient from JAPAN , weighting 154.3 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, infusion related reaction, malaise, myalgia, pyrexia, therapeutic response decreased. Remicade dosage: 17th Infusion; Only 33.5 Mg Actually Administered. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDONINE (Route Of Admin Is Dr) (View Predonine Review and Predonine Label ), TALION (View Talion Review and Talion Label ), ISOTONIC SODIUM CHLORIDE (View Isotonic Sodium Chloride Review and Isotonic Sodium Chloride Label ). Patient was hospitalized.

7019911-6 | Lung Disorder
on Sep 17, 2010 Female patient from UNITED STATES , weighting 71.21 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: lung disorder. Remicade dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).

7019910-4 | Albumin Urine Present, Cyanosis, Dyspnoea, Infusion Related Reaction, Pruritus, Tachycardia, Urine Ketone Body Present
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: albumin urine present, cyanosis, dyspnoea, infusion related reaction, pruritus, tachycardia, urine ketone body present on Sep 17, 2010 from HUNGARY Additional patient health information: Female patient , weighting 116.8 lb, was diagnosed with colitis ulcerative and. Remicade dosage: 5th Infusion. During the same period patient was treated with MESALAMINE (View Mesalamine Review and Mesalamine Label ).

7019909-8 | Systemic Lupus Erythematosus Rash
Adverse event was reported on Sep 17, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), prophylaxis, antibiotic prophylaxis and. Location: JAPAN , 68 years of age, weighting 94.80 lb, Patient experienced the following unwanted or unexpected effects: systemic lupus erythematosus rash. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ), NEOISCOTIN (View Neoiscotin Review and Neoiscotin Label ). Patient was hospitalized.

7018707-9 | Anaphylactic Reaction, Tuberculosis
on Sep 17, 2010 Female patient from FRANCE , 27 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). Patient had the following side effects: anaphylactic reaction, tuberculosis (What is tuberculosis?). Remicade dosage: . During the same period patient was treated with HUMIRA (View Humira Review and Humira Label ), PURINETHOL (View Purinethol Review and Purinethol Label ). Patient was hospitalized.

7018706-7 | Atypical Mycobacterial Infection
on Sep 17, 2010 Female patient from JAPAN , 53 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: atypical mycobacterial infection. Remicade dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

7018659-1 | Incision Site Infection, Intestinal Resection
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: incision site infection, intestinal resection on Sep 17, 2010 from CANADA Additional patient health information: Male patient , weighting 183.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and. Remicade dosage: . Patient was hospitalized.

7018577-9 | Anaphylactic Reaction, Anaphylactic Shock, Back Pain, Dyspnoea, Erythema, Hypotension, Infusion Related Reaction, Malaise, Tachycardia
Adverse event was reported on Sep 17, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with crohn's disease (What is crohn's disease?) and. Location: FRANCE , 29 years of age, weighting 110.2 lb, Patient had the following side effects: anaphylactic reaction, anaphylactic shock, back pain (What is back pain?), dyspnoea, erythema, hypotension, infusion related reaction, malaise, tachycardia.

7018520-2 | Abdominal Discomfort, Anaemia, Arthralgia, Hypotension, Incoherent, Leukocytosis, Oedema, Somnolence
on Sep 16, 2010 Female patient from PERU , 68 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: abdominal discomfort, anaemia, arthralgia, hypotension, incoherent, leukocytosis, oedema, somnolence. Remicade dosage: . During the same period patient was treated with THYROXIN (View Thyroxin Review and Thyroxin Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ), PLASIL (View Plasil Review and Plasil Label ), TRAMADOL (View Tramadol Review and Tramadol Label ). Patient was hospitalized.

7018483-X | Choroid Melanoma
on Sep 17, 2010 Male patient from BELGIUM , 64 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: choroid melanoma. Remicade dosage: . Patient was hospitalized.

7018482-8 | Blood Potassium Decreased, Fall, Urinary Tract Infection
Patient was taking Remicade (View Usage). Patient had the following side effects: blood potassium decreased, fall (What is fall?), urinary tract infection (What is urinary tract infection?) on Sep 17, 2010 from CANADA Additional patient health information: Female patient , weighting 253.5 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), NOVO HYDRAZIDE (View Novo-hydrazide Review and Novo-hydrazide Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ). Patient was hospitalized.

7018470-1 | Lymphocyte Count Decreased, Progressive Multifocal Leukoencephalopathy
Adverse event was reported on Sep 16, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: FRANCE , 60 years of age, After Remicade was administered, patient had the following side effects: lymphocyte count decreased, progressive multifocal leukoencephalopathy. Patient was hospitalized.

7018469-5 | Pancreatic Neoplasm
on Sep 14, 2010 Female patient from FRANCE , weighting 123.5 lb, was diagnosed with crohn's disease (What is crohn's disease?), pain (What is pain?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: pancreatic neoplasm. Remicade dosage: 21 Weeks Pregnant. During the same period patient was treated with SPASFON (View Spasfon Review and Spasfon Label ).

7018468-3 | Prostate Cancer
on Sep 16, 2010 Male patient from UNITED STATES , weighting 213.2 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient had the following side effects: prostate cancer (What is prostate cancer?). Remicade dosage: .

7018467-1 | Abscess, Fall, Incoherent, Joint Injury, Perforated Ulcer, Skin Laceration
Patient was taking Remicade (View Usage). After Remicade was administered, patient had the following side effects: abscess (What is abscess?), fall (What is fall?), incoherent, joint injury, perforated ulcer, skin laceration on Sep 17, 2010 from CANADA Additional patient health information: Female patient , weighting 147.7 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: . Patient was hospitalized.

7018466-X | Squamous Cell Carcinoma
Adverse event was reported on Sep 17, 2010 by a Male patient taking Remicade (View Usage) (Dosage: ) was diagnosed with hidradenitis (What is hidradenitis?) and. Location: UNITED STATES , 38 years of age, Patient experienced the following unwanted or unexpected effects: squamous cell carcinoma.

7018465-8 | Hepatic Cirrhosis, Hepatic Neoplasm Malignant
on Sep 17, 2010 Male patient from FRANCE , 68 years of age, was diagnosed with psoriasis and was treated with Remicade (View Usage). Patient had the following side effects: hepatic cirrhosis, hepatic neoplasm malignant. Remicade dosage: 7 Infusions. During the same period patient was treated with ENBREL (3 Months) (View Enbrel Review and Enbrel Label ).

7018004-1 | Abscess, Gastrointestinal Disorder
on Sep 17, 2010 Male patient from UNITED STATES , 30 years of age, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: abscess (What is abscess?), gastrointestinal disorder. Remicade dosage: .

7017899-5 | Ascites, Peritonitis, Pleural Effusion, Pulmonary Tuberculosis, Tuberculous Pleurisy
Patient was taking Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: ascites, peritonitis, pleural effusion, pulmonary tuberculosis, tuberculous pleurisy on Sep 16, 2010 from JAPAN Additional patient health information: Male patient , weighting 176.4 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Remicade dosage: . During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ), RIMATIL (View Rimatil Review and Rimatil Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ). Patient was hospitalized.

7017868-5 | Arthralgia, Arthritis, Lip Oedema, Myalgia, Pain In Jaw, Urticaria
Adverse event was reported on Sep 17, 2010 by a Female patient taking Remicade (View Usage) (Dosage: ) was diagnosed with crohn's disease (What is crohn's disease?), coronary artery disease (What is coronary artery disease?) and. Location: FRANCE , 52 years of age, weighting 99.21 lb, Patient had the following side effects: arthralgia, arthritis (What is arthritis?), lip oedema, myalgia, pain in jaw, urticaria. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

7017866-1 | Myopathy
on Sep 16, 2010 Female patient from SWEDEN , 41 years of age, was diagnosed with ankylosing spondylitis (What is ankylosing spondylitis?) and was treated with Remicade (View Usage). After Remicade was administered, patient had the following side effects: myopathy. Remicade dosage: .

7017758-8 | Pharyngeal Haemorrhage
on Sep 16, 2010 Female patient from JAPAN , 71 years of age, weighting 121.3 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Remicade (View Usage). Patient experienced the following unwanted or unexpected effects: pharyngeal haemorrhage. Remicade dosage: . During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ).

7017757-6 | Arthralgia, Uveitis
Patient was taking Remicade (View Usage). Patient had the following side effects: arthralgia, uveitis on Sep 16, 2010 from FRANCE Additional patient health information: Female patient , 37 years of age, . Remicade dosage: . During the same period patient was treated with METOJECT (View Metoject Review and Metoject Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), CONTRACEPTION (View Contraception Review and Contraception Label ), ATARAX (View Atarax Review and Atarax Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ).

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Remicade Questions, Answers, Feedback and Comments

Comments to date: 5. Page 1 of 1.

Tamara   Mesa, Arizona

11:20pm on Saturday, April 23rd, 2011


I have ulcerative colitis, I have had 9 treatments of Remicade and have decided to stop. I have a... read more »

Lavonna   oakhurst 

12:38pm on Friday, December 3rd, 2010

Put on Remicade for non FDA approved disease called hidradenitis, mine is severe, but, i never got b... read more »

Nathalie   Metro Manila

6:04am on Sunday, February 28th, 2010

I recieved Remicade as treatment for my Ulcerative Colitis and after the treatment my diarrhea has w... read more »

Gail James   Location unknown

4:02am on Thursday, November 20th, 2008

I have been on Remicade since July 08. I have had many skin rash-like outbreaks, like psoriasis and ... read more »

Carol Beaulieu   Location unknown

3:32pm on Friday, September 5th, 2008

Remicade treatments in 2003 for Crohn's disease. During administration of my third dose, I immediat... read more »

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 Remicade 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 Remicade quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Remicade 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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Remicade Reactions
Abdominal PainWhat is Abdominal pain?
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Asthenia
Back PainWhat is Back pain?
Breast CancerWhat is Breast cancer?
Chest Discomfort
Chest PainWhat is Chest pain?
Chills
Crohn's DiseaseWhat is Crohn's disease?
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Diarrhoea
Disseminated Tuberculosis
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Fatigue
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HeadacheWhat is Headache?
Infusion Related Reaction
Lupus-like Syndrome
Malaise
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Pneumocystis Jiroveci Pneumonia
PneumoniaWhat is Pneumonia?
Pulmonary Tuberculosis
Pyrexia
RashWhat is Rash?
SepsisWhat is Sepsis?
TuberculosisWhat is Tuberculosis?
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Remicade 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 Remicade 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!