LYMPHADENOPATHY MEDIASTINAL side effect
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Drugs associated with LYMPHADENOPATHY MEDIASTINAL
EFAVIRENZ GLEEVEC HUMIRA METHOTREXATE NUTROPIN REBIF REMICADE SUNITINIB TIKOSYNHumira Side Effects Report #5550143-4
Consumer or non-health professional from ITALY reported HUMIRA problem on Dec 03, 2007. Female patient, weighting 125.7 lb, was diagnosed with rheumatoid arthritis, hypertension, xerophthalmia, sleep disorder, prophylaxis against gastrointestinal ulcer, thrombosis prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: lymphadenopathy mediastinal, rectal cancer, . HUMIRA dosage: 40 MG. During the same period patient was treated with TAUXID, BISOPROLOL FUMARATE, DROP STAR TG, BROMAZEPAM, PARACETAMOL, PARCET, HEPARIN. Patient was hospitalized. Patient recovered.
Nutropin Side Effects Report #5407416-5
NUTROPIN AQ problem was reported by a Physician from UNITED STATES on Aug 01, 2007. Male patient was diagnosed with body height below normal and was treated with NUTROPIN AQ. After drug was administered, patient experienced the following problems/side effects: lymphadenopathy mediastinal, . NUTROPIN AQ dosage: 0.6 MG, QD. During the same period patient was treated with SINGULAIR, ADDERALL, VITAMIN CAP. Patient recovered.
Humira Side Effects Report #5361319-3
Consumer or non-health professional from ITALY reported HUMIRA problem on June 13, 2007. Female patient, weighting 125.7 lb, was diagnosed with rheumatoid arthritis, hypertension, xerophthalmia, sleep disorder, prophylaxis against gastrointestinal ulcer, thrombosis prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: lymphadenopathy mediastinal, rectal cancer, . HUMIRA dosage: 40 MG. During the same period patient was treated with TAUXID, BISOPROLOL FUMARATE, DROP STAR TG, BROMAZEPAM, PARACETAMOL, PARCET, HEPARIN. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5569725-9
HUMIRA problem was reported by a Consumer or non-health professional from SPAIN on Dec 12, 2007. Male patient, weighting 176.4 lb, was diagnosed with rheumatoid arthritis, hypertension, prophylaxis against gastrointestinal ulcer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, lymphadenopathy mediastinal, red blood cell sedimentation rate increased, sputum culture positive, . HUMIRA dosage: unknown. During the same period patient was treated with DEFLAZACORT, NIFEDIPINE, MODURETIC, ACETAMINOPHEN, CELECOXIB, ACETYLSALICYLIC ACID SRT, CALCEVITA, OMEPRAZOLE. Patient recovered.
Humira Side Effects Report #5576599-9
Consumer or non-health professional from SPAIN reported HUMIRA problem on Dec 20, 2007. Male patient, weighting 176.4 lb, was diagnosed with rheumatoid arthritis, hypertension, prophylaxis against gastrointestinal ulcer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, lymphadenopathy mediastinal, red blood cell sedimentation rate increased, . HUMIRA dosage: unknown. During the same period patient was treated with DEFLAZACORT, NIFEDIPINE, MODURETIC, ACETAMINOPHEN, CELECOXIB, ACETYLSALICYLIC ACID SRT, CALCEVITA, OMEPRAZOLE. Patient recovered.
Humira Side Effects Report #5505262-5
HUMIRA problem was reported by a Consumer or non-health professional from SPAIN on Oct 26, 2007. Male patient, weighting 176.4 lb, was diagnosed with rheumatoid arthritis, hypertension, prophylaxis against gastrointestinal ulcer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, lymphadenopathy mediastinal, red blood cell sedimentation rate increased, sputum culture positive, . HUMIRA dosage: unknown. During the same period patient was treated with DEFLAZACORT, NIFEDIPINE, MODURETIC, ACETAMINOPHEN, CELECOXIB, ACETYLSALICYLIC ACID SRT, CALCEVITA, OMEPRAZOLE. Patient recovered.
Humira Side Effects Report #5697648-3
Consumer or non-health professional from SPAIN reported HUMIRA problem on Mar 31, 2008. Male patient, weighting 176.4 lb, was diagnosed with rheumatoid arthritis, hypertension, prophylaxis against gastrointestinal ulcer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, lymphadenopathy mediastinal, mycobacterium avium complex infection, mycobacterium fortuitum infection, red blood cell sedimentation rate increased, . HUMIRA dosage: unknown. During the same period patient was treated with DEFLAZACORT, NIFEDIPINE, MODURETIC, PARACETAMOL, CELECOXIB, ACETYLSALICYLIC ACID SRT, CALCEVITA, OMEPRAZOLE. Patient recovered.
Humira Side Effects Report #5713550-2
HUMIRA problem was reported by a Consumer or non-health professional from SPAIN on Apr 16, 2008. Male patient, weighting 176.4 lb, was diagnosed with rheumatoid arthritis, hypertension, prophylaxis against gastrointestinal ulcer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, lymphadenopathy mediastinal, mycobacterium avium complex infection, mycobacterium fortuitum infection, red blood cell sedimentation rate increased, . HUMIRA dosage: unknown. During the same period patient was treated with DEFLAZACORT, NIFEDIPINE, MODURETIC, PARACETAMOL, CELECOXIB, ACETYLSALICYLIC ACID SRT, CALCEVITA, OMEPRAZOLE. Patient recovered.
Humira Side Effects Report #5303477-2
Physician from FRANCE reported HUMIRA problem on Apr 11, 2007. Female patient, weighting 116.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: lymphadenopathy, lymphadenopathy mediastinal, squamous cell carcinoma, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, CORTICOIDS, METHOTREXATE, PREDNISONE, FOLIC ACID. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5310232-6
HUMIRA problem was reported by a Physician from FRANCE on Apr 19, 2007. Female patient, weighting 116.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: lymphadenopathy, lymphadenopathy mediastinal, squamous cell carcinoma, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, FOLIC ACID, METHOTREXATE, PREDNISONE, CORTICOIDS. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5612251-9
Physician from UNITED STATES reported GLEEVEC problem on Jan 31, 2008. Male patient, 60 years of age, weighting 202.8 lb, was diagnosed with renal cell carcinoma and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fatigue, lymphadenopathy mediastinal, nausea, pleural effusion, rash, . GLEEVEC dosage: 600MG PER DAY PO. During the same period patient was treated with RAD, REQUIP, HYDROCHLOROTHIAZIDE, NEXIUM, IMODIUM, OXYCODONE, LYRICA, EFFEXOR. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5564555-6
REMICADE problem was reported by a Physician from ITALY on Dec 10, 2007. Male patient, 36 years of age, was diagnosed with psoriasis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: ascites, lymphadenopathy, lymphadenopathy mediastinal, pericardial effusion, pleural effusion, pulmonary tuberculosis, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Efavirenz Side Effects Report #5518519-9
Health Professional from JAPAN reported EFAVIRENZ problem on Nov 07, 2007. Male patient, 42 years of age, was diagnosed with hiv infection and was treated with EFAVIRENZ. After drug was administered, patient experienced the following problems/side effects: granulomatous liver disease, hepatomegaly, lymphadenopathy mediastinal, pyrexia, . EFAVIRENZ dosage: unknown. During the same period patient was treated with ZERIT, EPIVIR. Patient recovered.
Tikosyn Side Effects Report #5408634-2
TIKOSYN problem was reported by a Pharmacist from UNITED STATES on July 27, 2007. Male patient, weighting 163.1 lb, was diagnosed with atrial fibrillation and was treated with TIKOSYN. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, liver function test abnormal, lymphadenopathy mediastinal, . TIKOSYN dosage: unknown. During the same period patient was treated with COLACE, TEMAZEPAM, TYLENOL, VALSARTAN, ASCORBIC ACID, VITAMINS WITH MINERALS. Patient recovered.
Humira Side Effects Report #5762646-8
Consumer or non-health professional from GERMANY reported HUMIRA problem on May 30, 2008. Female patient, 47 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: lymph node tuberculosis, lymphadenopathy, lymphadenopathy mediastinal, . HUMIRA dosage: unknown. During the same period patient was treated with SULFAZALAZINE, PREDNISOLONE. Patient recovered.
Sunitinib Side Effects Report #5358328-7
SUNITINIB problem was reported by a Health Professional from UNITED STATES on June 14, 2007. Male patient, weighting 220.5 lb, was diagnosed with renal cancer metastatic and was treated with SUNITINIB. After drug was administered, patient experienced the following problems/side effects: haemoptysis, hilar lymphadenopathy, lymphadenopathy mediastinal, metastases to peripheral vascular system, . SUNITINIB dosage: 50 MG QDX28 DAYS PO. During the same period patient was treated with ATENOLOL, COMPAZINE, ZOFRAN, ALLEGRA. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5333447-X
Physician from UNITED STATES reported REBIF problem on May 10, 2007. Female patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: influenza like illness, lymphadenopathy, lymphadenopathy mediastinal, pain, sarcoidosis, treatment noncompliance, . REBIF dosage: unknown. Patient recovered.
Methotrexate Side Effects Report #5314622-7
METHOTREXATE problem was reported by a Consumer or non-health professional from FRANCE on Apr 19, 2007. Female patient, 58 years of age, was diagnosed with polyarthritis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: hypopharyngeal cancer, lymphadenopathy, lymphadenopathy mediastinal, oesophageal disorder, tumour invasion, . METHOTREXATE dosage: (15 MG, 1 IN 1 WK); ORAL. During the same period patient was treated with LEFLUNOMIDE, HUMIRA, FOLIC ACID, PREDNISONE. Patient recovered.