MOBILITY DECREASED side effect
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Drugs associated with MOBILITY DECREASED
ACLASTA ACTOS ADARTREL ALDURAZYME ALEVE AMBISOME AMLODIPINE APROVEL ARIMIDEX ARRANON ASPIRIN AVANDAMET AVANDIA AVELOX AVONEX AZATHIOPRINE BETAFERON BETASERON BONIVA BYETTA CANCIDAS CARBAMAZEPINE CHAMPIX CHANTIX CIPRO CIPROFLOXACIN CLOZARIL COLCHICINE COMTAN COREG COZAAR CRESTOR CYMBALTA DEPAKOTE DEROXAT DICLOFENAC DIDRONEL DYSPORT ENBREL ETANERCEPT ETONOGESIREL EXELON FEMARA FENTANYL FORTEO FOSAMAX FUROSEMIDE GADOLINIUM GADOLITE GENOX HEPARIN HUMALOG HUMIRA IBANDRONIC IMITREX INFLIXIMAB ISOSORBIDE LAMISIL LANTUS LEVAQUIN LIORESAL LIPITOR LYRICA MAGNEVIST METFORMIN MIRAPEX MIRENA MIRTAZAPINE MORPHINE NATALIZUMAB NEORAL NEUPRO NEXAVAR NEXIUM NICORETTE OLANZAPINE OLMESARTAN OMNISCAN ONDANSETRON OXYCODONE PANTOPRAZOLE PAROXETINE PHENYTOIN PRAVACHOL PRAVASTATIN QUILONORM REBIF REMICADE RENAGEL REQUIP REVITIO REVLIMID ROCEPHIN ROPINIROLE ROSIGLITAZONE ROZEREM SEROQUEL SEROXAT SIMVASTATIN SINEMET SUTENT TEMODAL TEMOZOLOMID THALOMID TOLTERODINE TOPIRAMATE TRAZODONE TYKERB TYSABRI VALPROATE VYTORIN WARFARIN ZETIA ZOCOR ZOLEDRONICMagnevist Side Effects Report #5649220-9
Consumer or non-health professional from UNITED STATES reported MAGNEVIST problem on Dec 05, 2007. Male patient, 49 years of age, was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . MAGNEVIST dosage: unknown. During the same period patient was treated with PROHANCE. Patient recovered.
Humira Side Effects Report #5666904-7
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2008. Male patient, weighting 146.1 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pain, . HUMIRA dosage: unknown. During the same period patient was treated with IBUPROFEN, BENAZEPRIL HYDROCHLORIDE. Patient recovered.
Tysabri Side Effects Report #5670053-1
Health Professional from IRELAND reported TYSABRI problem on Feb 25, 2008. Female patient, 23 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: mobility decreased, trigeminal neuralgia, vertigo, . TYSABRI dosage: unknown. Patient was hospitalized. Patient recovered.
Lipitor Side Effects Report #5671976-X
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2008. Male patient, 60 years of age, weighting 274.0 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle atrophy, pain in extremity, sleep disorder, . LIPITOR dosage: 10MG ONCE A DAY PO. Patient recovered.
Lyrica Side Effects Report #5677354-1
Consumer or non-health professional from UNITED STATES reported LYRICA problem on Mar 20, 2008. Female patient, 59 years of age, weighting 180.0 lb, was diagnosed with fibromyalgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: mobility decreased, oedema peripheral, . LYRICA dosage: unknown. During the same period patient was treated with AMBIEN, CYMBALTA, METHADON. Patient recovered.
Neoral Side Effects Report #5678918-1
NEORAL problem was reported by a Consumer or non-health professional from AUSTRALIA on Mar 13, 2008. Male patient, 55 years of age, was diagnosed with liver transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pain, upper limb fracture, . NEORAL dosage: unknown. Patient recovered.
Actos Side Effects Report #5590588-X
Physician from UNITED STATES reported ACTOS problem on Jan 04, 2008. Female patient, 73 years of age, was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pain in extremity, pulmonary oedema, . ACTOS dosage: unknown. During the same period patient was treated with AVANDIA. Patient was hospitalized. Patient died on 12/01/2007.
Sinemet Side Effects Report #5599744-8
SINEMET problem was reported by a Health Professional from UNITED STATES on Jan 16, 2008. Female patient, 70 years of age, was treated with SINEMET. After drug was administered, patient experienced the following problems/side effects: mobility decreased, mutism, . SINEMET dosage: 1 FORM = 50/12.5 MG TABLET. Patient recovered.
Forteo Side Effects Report #5564706-3
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Dec 04, 2007. Female patient was diagnosed with osteoporosis, pain, vitamin supplementation and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pain in extremity, . FORTEO dosage: unknown. During the same period patient was treated with DARVON, ASPIRIN, LOPRESSOR, FOLIC ACID, PREVACID. Patient recovered.
Revlimid Side Effects Report #5565452-2
REVLIMID problem was reported by a Physician from UNITED STATES on Dec 06, 2007. Male patient, 76 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . REVLIMID dosage: 25 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Betaseron Side Effects Report #5568246-7
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Dec 06, 2007. Female patient, 68 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, monoplegia, muscular weakness, . BETASERON dosage: unknown. Patient recovered.
Betaseron Side Effects Report #5572770-0
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2007. Female patient, 68 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, monoplegia, muscular weakness, . BETASERON dosage: unknown. Patient recovered.
Coreg Side Effects Report #5515036-7
Consumer or non-health professional from UNITED STATES reported COREG problem on Nov 27, 2006. Female patient, 82 years of age, was treated with COREG. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, pruritus, . COREG dosage: 25MG TWICE PER DAY. During the same period patient was treated with LASIX, ALDACTONE, PRILOSEC, PRAVASTATIN. Patient recovered.
Lyrica Side Effects Report #5529662-2
LYRICA problem was reported by a Physician from FRANCE on Nov 19, 2007. Female patient was diagnosed with facial neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . LYRICA dosage: DAILY DOSE:25MG. During the same period patient was treated with DEROXAT. Patient recovered.
Byetta Side Effects Report #5565725-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 29, 2007. Female patient, 77 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.
Olmesartan Side Effects Report #5480893-X
OLMESARTAN MEDOXOMIL problem was reported by a Consumer or non-health professional from JAPAN on Sept 19, 2007. Male patient, 35 years of age, weighting 191.8 lb, was diagnosed with self mutilation and was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: mobility decreased, overdose, shock, suicide attempt, vomiting, . OLMESARTAN MEDOXOMIL dosage: 74T (1480 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with ARTIST, ADALAT CR, DIOVAN, ALLOPURINOL. Patient recovered.
Omniscan Side Effects Report #5489236-9
Consumer or non-health professional from UNITED STATES reported OMNISCAN problem on July 11, 2007. Female patient, 34 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: mobility decreased, nephrogenic systemic fibrosis, renal failure, . OMNISCAN dosage: unknown. Patient recovered.
Natalizumab Side Effects Report #5490329-0
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 05, 2007. Male patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: mobility decreased, walking aid user, wheelchair user, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with AVONEX. Patient died on 09/01/2007.
Pravachol Side Effects Report #5444976-2
Health Professional from UNITED STATES reported PRAVACHOL problem on Sept 04, 2007. Female patient, 61 years of age, weighting 161.0 lb, was diagnosed with blood cholesterol increased and was treated with PRAVACHOL. After drug was administered, patient experienced the following problems/side effects: mobility decreased, musculoskeletal stiffness, myalgia, . PRAVACHOL dosage: 20 MG. DAILY PO. Patient recovered.
Forteo Side Effects Report #5446285-4
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 27, 2007. Female patient was diagnosed with fall and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle spasms, oesophageal obstruction, oesophageal rupture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5446562-7
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on June 20, 2007. Male patient, 25 years of age, weighting 259.9 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: mobility decreased, nausea, nightmare, sciatica, spinal disorder, vomiting, . CHANTIX dosage: unknown. During the same period patient was treated with WELLBUTRIN, EFFEXOR, TRILEPTAL, DOCUSATE, HYDROXYZINE, VITAMIN CAP, FLUPHENAZINE. Patient recovered.
Betaseron Side Effects Report #5447876-7
BETASERON problem was reported by a Consumer or non-health professional from CANADA on Aug 28, 2007. Female patient, 65 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Natalizumab Side Effects Report #5448398-X
Health Professional from UNITED STATES reported NATALIZUMAB problem on Aug 27, 2007. Female patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle atrophy, muscular weakness, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX. Patient was hospitalized. Patient recovered.
Ropinirole Side Effects Report #5450164-6
ROPINIROLE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 05, 2007. Female patient, 65 years of age, weighting 218.3 lb, was diagnosed with restless legs syndrome, pain, inflammation, hypothyroidism and was treated with ROPINIROLE. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . ROPINIROLE dosage: unknown. During the same period patient was treated with EZETIMIBE, IBUPROFEN, ISPAGHULA HUSK, LEVOTHYROXINE, ROSUVASTATIN. Patient recovered.
Mirtazapine Side Effects Report #5455161-2
Consumer or non-health professional from UNITED KINGDOM reported MIRTAZAPINE problem on Sept 10, 2007. Female patient, 35 years of age, was diagnosed with depression and was treated with MIRTAZAPINE. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle spasms, pain in extremity, white blood cell count increased, . MIRTAZAPINE dosage: 45 MG; QD; PO. During the same period patient was treated with SETAZINE. Patient recovered.
Gadolite Side Effects Report #5409295-9
GADOLITE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 07, 2007. Male patient, 38 years of age, weighting 155.0 lb, was diagnosed with nuclear magnetic resonance imaging and was treated with GADOLITE. After drug was administered, patient experienced the following problems/side effects: mobility decreased, skin disorder, skin lesion, . GADOLITE dosage: unknown. Patient recovered.
Cipro Side Effects Report #5410936-0
Consumer or non-health professional from UNITED STATES reported CIPRO problem on Aug 09, 2007. Female patient, 41 years of age, weighting 150.0 lb, was diagnosed with urinary tract infection and was treated with CIPRO. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pain, tendon disorder, . CIPRO dosage: unknown. Patient recovered.
Betaseron Side Effects Report #5377586-6
BETASERON problem was reported by a Consumer or non-health professional from CANADA on June 22, 2007. Female patient, 65 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Vytorin Side Effects Report #5377900-1
Health Professional from UNITED STATES reported VYTORIN problem on June 26, 2007. Male patient, 66 years of age, was diagnosed with blood cholesterol and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, . VYTORIN dosage: unknown. During the same period patient was treated with AVALIDE. Patient recovered.
Metformin Side Effects Report #5391391-6
METFORMIN problem was reported by a Consumer or non-health professional from GERMANY on May 04, 2007. Male patient, 57 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . METFORMIN dosage: unknown. During the same period patient was treated with NOVOMIX, SOLPRIN, LIPITOR, LERCANIDIPINE, PERGOLIDE MESYLATE, COVERSYL PLUS. Patient recovered.
Natalizumab Side Effects Report #5391855-5
Health Professional from UNITED STATES reported NATALIZUMAB problem on July 09, 2007. Female patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: mobility decreased, multiple sclerosis, muscular weakness, . NATALIZUMAB dosage: unknown. During the same period patient was treated with AVONEX. Patient was hospitalized. Patient recovered.
Ibandronic Side Effects Report #5400298-7
IBANDRONIC ACID problem was reported by a Physician from GERMANY on July 18, 2007. Female patient, 57 years of age, was diagnosed with osteoporosis postmenopausal and was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: mobility decreased, nausea, . IBANDRONIC ACID dosage: unknown. Patient recovered.
Betaseron Side Effects Report #5377586-6
Consumer or non-health professional from CANADA reported BETASERON problem on June 22, 2007. Female patient, 65 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Vytorin Side Effects Report #5377900-1
VYTORIN problem was reported by a Health Professional from UNITED STATES on June 26, 2007. Male patient, 66 years of age, was diagnosed with blood cholesterol and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscular weakness, . VYTORIN dosage: unknown. During the same period patient was treated with AVALIDE. Patient recovered.
Metformin Side Effects Report #5391391-6
Consumer or non-health professional from GERMANY reported METFORMIN problem on May 04, 2007. Male patient, 57 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . METFORMIN dosage: unknown. During the same period patient was treated with NOVOMIX, SOLPRIN, LIPITOR, LERCANIDIPINE, PERGOLIDE MESYLATE, COVERSYL PLUS. Patient recovered.
Natalizumab Side Effects Report #5391855-5
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on July 09, 2007. Female patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: mobility decreased, multiple sclerosis, muscular weakness, . NATALIZUMAB dosage: unknown. During the same period patient was treated with AVONEX. Patient was hospitalized. Patient recovered.
Ibandronic Side Effects Report #5400298-7
Physician from GERMANY reported IBANDRONIC ACID problem on July 18, 2007. Female patient, 57 years of age, was diagnosed with osteoporosis postmenopausal and was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: mobility decreased, nausea, . IBANDRONIC ACID dosage: unknown. Patient recovered.
Arranon Side Effects Report #5758590-2
ARRANON problem was reported by a Pharmacist from JAPAN on May 27, 2008. Male patient, 38 years of age, was diagnosed with prophylaxis of nausea and vomiting and was treated with ARRANON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pyrexia, vertigo, . ARRANON dosage: 2600MG PER DAY. During the same period patient was treated with KYTRIL, SEISHOKU, MEYLON, GLUCOSE, LANSOPRAZOLE, MAGMITT, ITRIZOLE. Patient recovered.
Lipitor Side Effects Report #5760478-8
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on May 29, 2008. Female patient, weighting 140.3 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: mobility decreased, myalgia, . LIPITOR dosage: unknown. During the same period patient was treated with SOTALOL, PRIMIDONE, WARFARIN, LORAZEPAM, LEVOTHROID, GLUCOSAMINE, CALCIUM WITH VITAMIN D, CALCIUM W. Patient recovered.
Tysabri Side Effects Report #5760549-6
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on May 23, 2008. Male patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . TYSABRI dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX. Patient died on 09/01/2007.
Humira Side Effects Report #5769562-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Apr 01, 2008. Female patient, weighting 165.1 lb, was diagnosed with psoriatic arthropathy, psoriasis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: mobility decreased, nausea, pain, procedural complication, . HUMIRA dosage: unknown. Patient recovered.
Thalomid Side Effects Report #5795303-2
THALOMID problem was reported by a Physician from UNITED STATES on June 19, 2008. Male patient, 57 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: mobility decreased, neuropathy peripheral, poems syndrome, . THALOMID dosage: 150 MG, ORAL, 100 MG, 1 IN 1 D, ORAL, 50-200 MG, DAILY, ORAL. Patient recovered.
Avonex Side Effects Report #5729782-3
Consumer or non-health professional from reported AVONEX problem on Apr 21, 2008. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: mobility decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Arranon Side Effects Report #5736432-9
ARRANON problem was reported by a Pharmacist from JAPAN on May 08, 2008. Male patient, 38 years of age, was treated with ARRANON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, pyrexia, vertigo, . ARRANON dosage: 2600MG PER DAY. Patient recovered.
Lipitor Side Effects Report #5739323-2
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on May 07, 2008. Male patient, weighting 186.4 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle disorder, . LIPITOR dosage: unknown. During the same period patient was treated with DOXAZOSIN MESYLATE, LISINOPRIL. Patient recovered.
Betaseron Side Effects Report #5744150-6
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2008. Female patient, 68 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: mobility decreased, monoplegia, muscular weakness, . BETASERON dosage: unknown. Patient recovered.
Neupro Side Effects Report #5748397-4
Physician from UNITED STATES reported NEUPRO problem on May 02, 2008. Male patient, 73 years of age, was diagnosed with parkinson's disease and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: mobility decreased, transient ischaemic attack, . NEUPRO dosage: 8MG/ 24H, 1 IN 1 D, TRANSDERMAL; 12 MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with STALEVO, TOPROL, LOTENSIN, IMDUR, HYDROCHLOROTHIAZIDE, ASPIRIN. Patient was hospitalized. Patient recovered.
Magnevist Side Effects Report #5750772-9
MAGNEVIST problem was reported by a Consumer or non-health professional from UNITED STATES on May 06, 2008. Male patient, 63 years of age, weighting 249.1 lb, was diagnosed with nuclear magnetic resonance imaging abdominal and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: mobility decreased, muscle tightness, . MAGNEVIST dosage: TOTAL DAILY DOSE: 20 ML UNIT DOSE: 20 ML. During the same period patient was treated with THYROID, PROPECIA, TESTOSTERONE GH. Patient recovered.
Rebif Side Effects Report #5757257-4
Health Professional from UNITED STATES reported REBIF problem on Mar 15, 2007. Female patient, 55 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: mobility decreased, multiple sclerosis relapse, muscular weakness, urinary incontinence, urinary tract infection, . REBIF dosage: unknown. During the same period patient was treated with BACLOFEN, LEXAPRO, DIOVAN, ZANTAC, VITAMIN B12. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5758668-3
REBIF problem was reported by a Physician from UNITED STATES on June 22, 2007. Female patient, 25 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: mobility decreased, motor dysfunction, multiple sclerosis relapse, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5758681-6
Physician from UNITED STATES reported REBIF problem on July 09, 2007. Male patient, 60 years of age, weighting 165.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: mobility decreased, multiple sclerosis relapse, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.