ARTHRITIS REACTIVE side effect
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Drugs associated with ARTHRITIS REACTIVE
ACCUTANE BOTOX CIPROFLOXACIN CIPROXIN CONCOR ENBREL INFLIXIMAB MEBENDAZOLE NUTROPIN RECLAST VALPROICBotox Side Effects Report #5679677-9
Physician from UNITED STATES reported BOTOX COSMETIC problem on Mar 17, 2008. Female patient was diagnosed with skin wrinkling and was treated with BOTOX COSMETIC. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, . BOTOX COSMETIC dosage: unknown. Patient recovered.
Nutropin Side Effects Report #5683009-X
NUTROPIN AQ problem was reported by a Physician from UNITED STATES on Mar 19, 2008. Male patient was treated with NUTROPIN AQ. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, . NUTROPIN AQ dosage: 1 MG, 7/WEEK. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5606119-1
Consumer or non-health professional from UNITED KINGDOM reported CIPROFLOXACIN problem on Jan 11, 2008. Female patient, 41 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, . CIPROFLOXACIN dosage: 500 MG TWICE DAILY ORAL. Patient was hospitalized. Patient recovered.
Concor Side Effects Report #5556089-X
CONCOR COR problem was reported by a Consumer or non-health professional from GERMANY on Dec 10, 2007. Female patient, 48 years of age, was treated with CONCOR COR. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, c-reactive protein increased, inflammation, musculoskeletal stiffness, myalgia, pain in extremity, pyrexia, . CONCOR COR dosage: 5 MG, BID. Patient was hospitalized. Patient recovered.
Infliximab Side Effects Report #5402107-9
Health Professional from UNITED KINGDOM reported INFLIXIMAB problem on July 20, 2007. Female patient, weighting 188.5 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, pyrexia, . INFLIXIMAB dosage: unknown. Patient was hospitalized. Patient recovered.
Enbrel Side Effects Report #5377133-9
ENBREL problem was reported by a Health Professional from UNITED KINGDOM on June 27, 2007. Female patient, weighting 118.4 lb, was diagnosed with rheumatoid arthritis, gastrooesophageal reflux disease and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, chills, erythema, feeling cold, injection site pain, joint swelling, nausea, vomiting, . ENBREL dosage: unknown. During the same period patient was treated with CALCICHEW, METHOTREXATE, FOLIC ACID, OMEPRAZOLE, PREDNISOLONE. Patient recovered.
Enbrel Side Effects Report #5377133-9
Health Professional from UNITED KINGDOM reported ENBREL problem on June 27, 2007. Female patient, weighting 118.4 lb, was diagnosed with rheumatoid arthritis, gastrooesophageal reflux disease and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, chills, erythema, feeling cold, injection site pain, joint swelling, nausea, vomiting, . ENBREL dosage: unknown. During the same period patient was treated with CALCICHEW, METHOTREXATE, FOLIC ACID, OMEPRAZOLE, PREDNISOLONE. Patient recovered.
Nutropin Side Effects Report #5694732-5
NUTROPIN AQ problem was reported by a Physician from UNITED STATES on Mar 26, 2008. Male patient, weighting 42.11 lb, was treated with NUTROPIN AQ. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, . NUTROPIN AQ dosage: 1 MG, 7/WEEK. During the same period patient was treated with AMLODIPINE, CEPHALEXIN, FERROUS SULPHATE, PREDNISONE, SEPTRA, TACROLIMUS. Patient was hospitalized. Patient recovered.
Mebendazole Side Effects Report #5370093-6
Physician from UNITED KINGDOM reported MEBENDAZOLE problem on June 15, 2007. Female patient, weighting 5.16 lb, was treated with MEBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: arthritis reactive, arthropathy, hip dysplasia, strabismus, upper respiratory tract infection, . MEBENDAZOLE dosage: unknown. Patient recovered.
Ciprofloxacin Side Effects Report #5579354-9
CIPROFLOXACIN problem was reported by a Health Professional from UNITED KINGDOM on Dec 27, 2007. Female patient, 41 years of age, weighting 149.9 lb, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye discharge, eye inflammation, hypersensitivity, osteitis, pain in extremity, . CIPROFLOXACIN dosage: unknown. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5581548-3
Health Professional from UNITED KINGDOM reported CIPROFLOXACIN problem on Jan 02, 2008. Female patient, 41 years of age, weighting 149.9 lb, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye discharge, eye inflammation, hypersensitivity, osteitis, pain in extremity, . CIPROFLOXACIN dosage: TOTAL DAILY DOSE: 1000 MG UNIT DOSE: 500 MG. Patient was hospitalized and became disabled. Patient recovered.
Ciprofloxacin Side Effects Report #5588201-0
CIPROFLOXACIN problem was reported by a Health Professional from UNITED KINGDOM on Dec 27, 2007. Female patient, 41 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: abasia, arthritis reactive, hypersensitivity, kidney infection, . CIPROFLOXACIN dosage: 500 MG TWICE DAILY ORAL. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5588228-9
Consumer or non-health professional from UNITED KINGDOM reported CIPROFLOXACIN problem on Dec 24, 2007. Female patient, 41 years of age, weighting 149.9 lb, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: abasia, arthritis reactive, back pain, eye swelling, kidney infection, ocular hyperaemia, oedema peripheral, . CIPROFLOXACIN dosage: 500 MG - BID. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5593201-0
CIPROFLOXACIN problem was reported by a Health Professional from UNITED KINGDOM on Jan 11, 2008. Female patient, 41 years of age, weighting 149.9 lb, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye discharge, eye inflammation, hypersensitivity, osteitis, pain in extremity, . CIPROFLOXACIN dosage: TOTAL DAILY DOSE: 1000 MG UNIT DOSE: 500 MG. Patient was hospitalized and became disabled. Patient recovered.
Ciprofloxacin Side Effects Report #5593634-2
Health Professional from UNITED KINGDOM reported CIPROFLOXACIN problem on Jan 11, 2008. Female patient was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye discharge, eye inflammation, eye swelling, hypersensitivity, ocular hyperaemia, . CIPROFLOXACIN dosage: 500 MG, BID. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5599471-7
CIPROFLOXACIN problem was reported by a Health Professional from UNITED KINGDOM on Jan 02, 2008. Female patient, 41 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye swelling, hypersensitivity, ocular hyperaemia, osteitis, pain in extremity, . CIPROFLOXACIN dosage: 500 MG; TWICE A DAY; ORAL. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5605608-3
Consumer or non-health professional from UNITED KINGDOM reported CIPROFLOXACIN problem on Jan 02, 2008. Female patient, 41 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, back pain, eye swelling, hypersensitivity, ocular hyperaemia, osteitis, pain in extremity, . CIPROFLOXACIN dosage: 500 MG; TWICE A DAY, ORAL. Patient was hospitalized. Patient recovered.
Ciproxin Side Effects Report #5447311-9
CIPROXIN problem was reported by a Physician from UNITED KINGDOM on Sept 05, 2007. Female patient, 53 years of age, was diagnosed with kidney infection and was treated with CIPROXIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, joint swelling, oedema peripheral, pain in extremity, tendon disorder, tendon pain, tenosynovitis, walking disability, . CIPROXIN dosage: unknown. Patient recovered.
Reclast Side Effects Report #5380516-4
Physician from UNITED KINGDOM reported RECLAST problem on June 27, 2007. Female patient was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, influenza like illness, joint effusion, joint swelling, joint warmth, nausea, oral pain, pyrexia, . RECLAST dosage: 4MG. During the same period patient was treated with LANSOPRAZOLE, INDAPAMIDE, VALSARTAN, CLIMAVAL. Patient recovered.
Reclast Side Effects Report #5380516-4
RECLAST problem was reported by a Physician from UNITED KINGDOM on June 27, 2007. Female patient was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis reactive, influenza like illness, joint effusion, joint swelling, joint warmth, nausea, oral pain, pyrexia, . RECLAST dosage: 4MG. During the same period patient was treated with LANSOPRAZOLE, INDAPAMIDE, VALSARTAN, CLIMAVAL. Patient recovered.
Accutane Side Effects Report #5738913-0
Physician from UNITED STATES reported ACCUTANE problem on May 05, 2008. Male patient, weighting 140.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthritis reactive, colitis, colitis ulcerative, emotional distress, inflammatory bowel disease, intestinal obstruction, . ACCUTANE dosage: unknown. During the same period patient was treated with TETRACYCLIN, ERYTHROMYCIN, BENZAMYCIN, RETIN. Patient recovered.
Accutane Side Effects Report #5746173-X
ACCUTANE problem was reported by a Physician from UNITED STATES on May 12, 2008. Male patient, weighting 140.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthritis reactive, colitis, colitis ulcerative, emotional distress, inflammatory bowel disease, intestinal obstruction, . ACCUTANE dosage: unknown. During the same period patient was treated with TETRACYCLIN, ERYTHROMYCIN, BENZAMYCIN, RETIN. Patient recovered.
Accutane Side Effects Report #5709150-0
Physician from UNITED STATES reported ACCUTANE problem on Apr 07, 2008. Male patient, weighting 140.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arthritis reactive, colitis, colitis ulcerative, emotional distress, inflammatory bowel disease, intestinal obstruction, . ACCUTANE dosage: unknown. During the same period patient was treated with TETRACYCLIN, ERYTHROMYCIN, BENZAMYCIN, RETIN. Patient recovered.
Accutane Side Effects Report #5675629-3
ACCUTANE problem was reported by a Physician from UNITED STATES on Mar 12, 2008. Male patient, 24 years of age, weighting 179.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, arthritis reactive, attention deficit/hyperactivity disorder, colitis, crohn's disease, depression, inflammatory bowel disease, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.
Accutane Side Effects Report #5612039-9
Physician from UNITED STATES reported ACCUTANE problem on Jan 24, 2008. Male patient, 24 years of age, weighting 179.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, arthritis reactive, attention deficit/hyperactivity disorder, colitis, crohn's disease, depression, inflammatory bowel disease, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.
Ciprofloxacin Side Effects Report #5569624-2
CIPROFLOXACIN problem was reported by a Health Professional from UNITED KINGDOM on Dec 04, 2007. Female patient, 41 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: abasia, arthralgia, arthritis reactive, back pain, eye discharge, eye inflammation, musculoskeletal stiffness, . CIPROFLOXACIN dosage: 1000 MG (500 MG, 2 IN 1 D) ORAL. Patient was hospitalized. Patient recovered.
Accutane Side Effects Report #5489673-2
Physician from UNITED STATES reported ACCUTANE problem on Oct 11, 2007. Male patient, 24 years of age, weighting 179.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, arthritis reactive, attention deficit/hyperactivity disorder, colitis, crohn's disease, depression, inflammatory bowel disease, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.
Accutane Side Effects Report #5766512-3
ACCUTANE problem was reported by a Physician from UNITED STATES on May 30, 2008. Male patient, weighting 140.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anorexia, arthritis reactive, colitis, colitis ulcerative, dehydration, emotional distress, inflammatory bowel disease, intestinal obstruction, . ACCUTANE dosage: unknown. During the same period patient was treated with TETRACYCLIN, ERYTHROMYCIN, BENZAMYCIN, RETIN. Patient was hospitalized. Patient recovered.
Accutane Side Effects Report #5738914-2
Physician from UNITED STATES reported ACCUTANE problem on May 05, 2008. Male patient, weighting 179.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, arthritis reactive, attention deficit/hyperactivity disorder, colitis, cough, crohn's disease, depression, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.
Valproic Side Effects Report #5746108-X
VALPROIC ACID problem was reported by a Physician from FRANCE on May 15, 2008. Male patient, weighting 7.14 lb, was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, aortogram abnormal, arthritis reactive, congenital aortic anomaly, congenital eye disorder, congenital hair disorder, congenital nose malformation, cough, . VALPROIC ACID dosage: unknown. During the same period patient was treated with VALPROIC ACID, LAMOTRIGINE. Patient recovered.
Accutane Side Effects Report #5328471-7
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on May 08, 2007. Male patient, 24 years of age, weighting 179.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, arthritis reactive, attention deficit/hyperactivity disorder, colitis, crohn's disease, depression, inflammatory bowel disease, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.