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side effects patient, 79 years of age, weighting 178.0 lb, was diagnosed with rheumatoid arthritis and took Humira 40 mg/ 0.8 ml pre-filled syringe (humira) (adali. View more Serious Adverse Events reported to FDA.

List of Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu Adverse Effects reported to US Food and Drug Administration (FDA)

Injection Site Erythema, Injection Site Nodule, Injection Site Pruritus, Injection Site Rash, Injection Site Swelling (4554437-0)
on Nov 04, 2004 Female patient from , 79 years of age, weighting 178.0 lb, was diagnosed with
  • rheumatoid arthritis
and was treated with Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu. Patient experienced the following unwanted or unexpected effects: injection site erythema, injection site nodule, injection site pruritus, injection site rash, injection site swelling. Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu dosage: 40 Mg, 1 In 2 Wk, Subcutaneous.
Patient also using the following medications:
  • Hydrophen
  • Paracetamol
  • Prednisone
  • Folic Acid
  • Calcium Gluconate
  • Albuterol
  • Asthma Cor
  • Amlodipine Besylate


Mood Altered (4554432-1)
Patient was taking Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu. Patient had the following side effects: mood altered on Oct 04, 2004 from Additional patient health information: Female patient , 49 years of age, weighting 190.0 lb, was diagnosed with
  • rheumatoid arthritis
and. Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu dosage: 40 Mg, 1 In 2 Wk, Subcutaneous.
Patient also using the following medications:
  • Levothyroxine Sodium


Cellulitis, Phlebitis (4554429-1)
Adverse event was reported on Sep 29, 2004 by a Female patient taking Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu (Dosage: 40 Mg, 1 In 2 Wk, Injection) was diagnosed with
  • rheumatoid arthritis
and. Location: , 62 years of age, weighting 148.0 lb, After Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu was administered, patient had the following side effects: cellulitis, phlebitis.
Patient also using the following medications:
  • Co-diovan
  • Hydrochlorothiazide
  • Ibuprofen
  • Zolpidem Tartrate


Arthralgia, Joint Swelling, Musculoskeletal Stiffness (4554385-6)
on Oct 04, 2004 Female patient from , 59 years of age, weighting 146.0 lb, was diagnosed with
  • rheumatoid arthritis
and was treated with Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu. Patient experienced the following unwanted or unexpected effects: arthralgia, joint swelling, musculoskeletal stiffness. Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu dosage: 40 Mg, 1 In 2 Wk, Subcutaneous.
Patient also using the following medications:
  • Methotrexate
  • Lescol Xl
  • Omeprazole
  • Amitriptyline
  • Celecoxib
  • Risedronate Sodium
  • Folic Acid
  • Fluoxetine Hydrochloride



Libido Decreased (4554384-4)
on Oct 04, 2004 Female patient from , 39 years of age, was diagnosed with
  • rheumatoid arthritis
and was treated with Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu. Patient had the following side effects: libido decreased. Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu dosage: 40 Mg, 1 In 2 Wk, Subcutaneous.

Burning Sensation (4554382-0)
Patient was taking Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu. After Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu was administered, patient had the following side effects: burning sensation on Sep 30, 2004 from Additional patient health information: Female patient , 50 years of age, was diagnosed with
  • rheumatoid arthritis
and. Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu dosage: 40 Mg, 1 In 2 Wk, Subcutaneous.
Patient also using the following medications:
  • Hydrochlorothiazide
  • Valproate Sodium
  • Manaprin
  • Fluoxetine Hydrochloride


Nasopharyngitis (4554372-8)
Adverse event was reported on Oct 04, 2004 by a Female patient taking Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu (Dosage: 40 Mg, 1 In 2 Wk, Subcutaneous) was diagnosed with
  • rheumatoid arthritis
and. Location: , 53 years of age, weighting 152.0 lb, Patient experienced the following unwanted or unexpected effects: nasopharyngitis.
Patient also using the following medications:
  • Atenolol
  • Prednisone
  • Methotrexate


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Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu Information

More About Humira 40 mg/ 0.8 ml pre-filled syringe (humira) (adalimumab) (adalimu

Side Effects reported to FDA: 7. View FDA Adverse Reports

Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu safety alerts: No

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further research and contacting my doctor

When did you start feeling unusual symptoms? what was the first symptom? Did your symptoms get worse over time? Did you have similar symptoms before using Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu? What did Your doctor say? Share Your Story

Humira 40 Mg/ 0.8 Ml Pre-filled Syringe (humira) (adalimumab) (adalimu Adverse Reactions

Arthralgia ( 1 Reports)

Burning Sensation ( 1 Reports)

Cellulitis ( 1 Reports)

Injection Site Erythema ( 1 Reports)

Injection Site Nodule ( 1 Reports)

Injection Site Pruritus ( 1 Reports)

Injection Site Rash ( 1 Reports)

Injection Site Swelling ( 1 Reports)

Joint Swelling ( 1 Reports)

Libido Decreased ( 1 Reports)

Mood Altered ( 1 Reports)

Musculoskeletal Stiffness ( 1 Reports)

Nasopharyngitis ( 1 Reports)

Phlebitis ( 1 Reports)

side effects
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