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CENTRAL NERVOUS SYSTEM LESION side effect

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Duragesic Side Effects Report #5669094-X
Physician from UNITED STATES reported DURAGESIC problem on Mar 10, 2008. Female patient, 55 years of age, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, cerebral haemorrhage, haemangioma, migraine, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5616918-8
REBIF problem was reported by a Physician from SLOVENIA on Jan 18, 2008. Female patient, 32 years of age, weighting 136.7 lb, was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Fabrazyme Side Effects Report #5625166-7
Physician from GERMANY reported FABRAZYME problem on Jan 25, 2008. Female patient, 43 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, cerebral infarction, . FABRAZYME dosage: unknown. During the same period patient was treated with LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Dalteparin Side Effects Report #5639070-1
DALTEPARIN problem was reported by a Physician from CZECH REPUBLIC on Feb 11, 2008. Female patient, 24 years of age, was diagnosed with cerebral venous thrombosis and was treated with DALTEPARIN. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, coma, condition aggravated, . DALTEPARIN dosage: unknown. During the same period patient was treated with PROGESTERONE, ANTIBIOTICS. Patient was hospitalized. Patient recovered.


Fabrazyme Side Effects Report #5646798-6
Physician from GERMANY reported FABRAZYME problem on Feb 14, 2008. Female patient, 43 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, cerebral infarction, cerebrovascular accident, sudden hearing loss, tinnitus, . FABRAZYME dosage: 70 MG, Q2W, INTRAVENOUS. During the same period patient was treated with LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Copaxone Side Effects Report #5633746-8
COPAXONE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2007. Female patient was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, optic neuritis, . COPAXONE dosage: 20 MG, SUBCUTANEOUS. Patient recovered.

Copaxone Side Effects Report #5633766-3
Health Professional from UNITED STATES reported COPAXONE problem on Feb 01, 2007. Female patient, child 10 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D), SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5541455-9
REMICADE problem was reported by a Physician from SPAIN on Nov 29, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, hemiparesis, . REMICADE dosage: unknown. Patient recovered.

Remicade Side Effects Report #5545574-2
Physician from SPAIN reported REMICADE problem on Nov 30, 2007. Female patient, 49 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, hemiparesis, tuberculosis skin test positive, . REMICADE dosage: unknown. During the same period patient was treated with DACORTIN, METHOTREXATE, CEMIDON. Patient was hospitalized. Patient recovered.


Betaseron Side Effects Report #5450409-2
BETASERON problem was reported by a Health Professional from UNITED STATES on Aug 31, 2007. Female patient, 57 years of age, weighting 170.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, cervical myelopathy, chills, injection site bruising, . BETASERON dosage: unknown. During the same period patient was treated with KEPPRA, TOPROL, NORVASC, LASIX, LUNESTA. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5413469-0
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Aug 03, 2007. Female patient, weighting 155.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, grand mal convulsion, pneumonia aspiration, type 2 diabetes mellitus, . REMICADE dosage: unknown. During the same period patient was treated with ASPIRIN, METHOTREXATE, LIPITOR, ATIVAN, ZOLOFT, LOPRESSOR, ANALAPRIL, LYRICA. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5731748-4
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2008. Female patient, 28 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, chorea, convulsion, dysphonia, . TYSABRI dosage: unknown. During the same period patient was treated with ANTIDEPRESSANTS. Patient recovered.

Avonex Side Effects Report #5734447-8
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 24, 2008. Female patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, feeling hot, intervertebral disc protrusion, sensory disturbance, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5738060-8
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2008. Female patient, weighting 171.1 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5740457-7
Consumer or non-health professional from reported AVONEX problem on May 01, 2008. Female patient, 23 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, headache, hypoaesthesia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5747451-0
ACCUTANE problem was reported by a Health Professional from UNITED STATES on May 14, 2008. Male patient, weighting 162.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, chronic sinusitis, colitis, colitis ulcerative, colonic polyp, crohn's disease, diverticulitis, dry mouth, feeling of despair, . ACCUTANE dosage: unknown. During the same period patient was treated with ZITHROMAX, ACCUPRIL, PERCOCET, TRIAMCINOLONE, LIBRAX. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5701509-0
Physician from UNITED STATES reported REBIF problem on Mar 27, 2008. Female patient, 26 years of age, weighting 130.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, dehydration, dizziness, mood swings, muscular weakness, presyncope, white blood cell count decreased, . REBIF dosage: unknown. During the same period patient was treated with ORAL CONTRACEPTIVES. Patient was hospitalized. Patient recovered.

Albendazole Side Effects Report #5714641-2
ALBENDAZOLE problem was reported by a Health Professional from NEPAL on Apr 16, 2008. Female patient, 35 years of age, weighting 99.21 lb, was treated with ALBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, cerebrovascular accident, dehydration, dizziness, headache, intracranial pressure increased, ischaemic cerebral infarction, loss of consciousness, vomiting, . ALBENDAZOLE dosage: unknown. During the same period patient was treated with DIETHYLCARBAMAZINE CITRATE. Patient was hospitalized. Patient died on 06/17/2007.

Avonex Side Effects Report #5724919-4
Consumer or non-health professional from reported AVONEX problem on Apr 17, 2008. Female patient, 23 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, headache, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Copaxone Side Effects Report #5363031-3
COPAXONE problem was reported by a Consumer or non-health professional from UNITED STATES on June 04, 2007. Female patient was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . COPAXONE dosage: 20 MG, SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Carbatrol Side Effects Report #5371583-2
Physician from JAPAN reported CARBATROL problem on June 12, 2007. Male patient, 32 years of age, was diagnosed with neuralgia and was treated with CARBATROL. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . CARBATROL dosage: unknown. Patient recovered.

Lyrica Side Effects Report #5319410-3
LYRICA problem was reported by a Physician from UNITED STATES on Apr 30, 2007. Female patient, weighting 214.1 lb, was diagnosed with back pain, radicular pain and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, conversion disorder, depression, pain, post-traumatic stress disorder, speech disorder, . LYRICA dosage: unknown. During the same period patient was treated with LEXAPRO, DARVOCET. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5288218-X
Health Professional from UNITED STATES reported ORTHO EVRA problem on Apr 02, 2007. Female patient, weighting 171.1 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5290586-X
TACROLIMUS problem was reported by a Physician from CANADA on Mar 30, 2007. Female patient, weighting 128.5 lb, was diagnosed with prophylaxis against transplant rejection and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . TACROLIMUS dosage: unknown. During the same period patient was treated with ZENAPAX, PREDNISONE, MYCOPHENOLATE MOFETIL. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5298567-7
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 30, 2007. Female patient, 61 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, hypertension, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5301158-2
LYRICA problem was reported by a Physician from UNITED STATES on Apr 10, 2007. Female patient, weighting 214.1 lb, was diagnosed with back pain, radicular pain and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, conversion disorder, depression, pain, post-traumatic stress disorder, speech disorder, . LYRICA dosage: unknown. During the same period patient was treated with LEXAPRO, DARVOCET. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5276842-X
Consumer or non-health professional from UNITED STATES reported REBIF problem on Jan 05, 2007. Male patient, 42 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: central nervous system lesion, . REBIF dosage: unknown. During the same period patient was treated with NAPROXEN. Patient recovered.

Fabrazyme Side Effects Report #5671586-4
FABRAZYME problem was reported by a Physician from GERMANY on Mar 06, 2008. Female patient, 43 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: amnesia, central nervous system lesion, cerebral infarction, cerebrovascular accident, sudden hearing loss, tinnitus, . FABRAZYME dosage: 70 MG, Q2W, INTRAVENOUS. During the same period patient was treated with LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Naglazyme Side Effects Report #5613391-0
Physician from BRAZIL reported NAGLAZYME problem on Jan 11, 2008. Male patient, child 7 years of age, weighting 32.19 lb, was diagnosed with mucopolysaccharidosis vi and was treated with NAGLAZYME. After drug was administered, patient experienced the following problems/side effects: abasia, central nervous system lesion, clonus, condition aggravated, csf protein increased, hyperreflexia, hypotonia, meningeal disorder, muscle spasticity, . NAGLAZYME dosage: 1.5 ML;QM;INTH, 15 MG;X1;IV. Patient recovered.

Betaseron Side Effects Report #5409001-8
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on July 26, 2007. Female patient, 61 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: asthenia, central nervous system lesion, memory impairment, nervous system disorder, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Norditropin Side Effects Report #5780066-7
Health Professional from UNITED KINGDOM reported NORDITROPIN problem on June 09, 2008. Male patient, child 12 years of age, was diagnosed with growth hormone deficiency and was treated with NORDITROPIN. After drug was administered, patient experienced the following problems/side effects: astrocytoma, central nervous system lesion, . NORDITROPIN dosage: 1 MG, QD. During the same period patient was treated with TRIPTORELIN. Patient recovered.

Tysabri Side Effects Report #5792225-8
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2008. Female patient, 36 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, central nervous system lesion, cough, granulocytopenia, influenza, malaise, multiple sclerosis relapse, nasopharyngitis, pharyngitis streptococcal, . TYSABRI dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX. Patient recovered.

Avonex Side Effects Report #5735090-7
Physician from UNITED STATES reported AVONEX problem on Apr 29, 2008. Female patient, 51 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: breast disorder female, central nervous system lesion, depression, precancerous cells present, schizophrenia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5743376-5
BOTOX problem was reported by a Physician from UNITED STATES on May 15, 2008. Male patient, 63 years of age, weighting 254.0 lb, was diagnosed with dystonia and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: autoimmune disorder, central nervous system lesion, condition aggravated, csf immunoglobulin increased, dementia, encephalitis allergic, encephalopathy, hiccups, postoperative wound infection, . BOTOX dosage: unknown. Patient was hospitalized. Patient recovered.

Darunavir Side Effects Report #5744203-2
Pharmacist from UNITED STATES reported DARUNAVIR problem on May 15, 2008. Male patient, 57 years of age, weighting 147.7 lb, was diagnosed with hiv infection and was treated with DARUNAVIR. After drug was administered, patient experienced the following problems/side effects: burkitt's lymphoma, central nervous system lesion, neuropathy peripheral, . DARUNAVIR dosage: 600MG Q12H PO. During the same period patient was treated with RALTEGRAVIR, TRIMETHOPRIM, TENOFOVIR, RITONOVIR. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5752076-7
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2008. Female patient, 49 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: brain oedema, central nervous system lesion, cognitive disorder, coma, gait disturbance, loss of consciousness, muscle rigidity, nuclear magnetic resonance imaging abnormal, progressive multifocal leukoencephalopathy, . TYSABRI dosage: 300 MG;QM;IV. Patient was hospitalized. Patient died on 04/28/2008.

Rebif Side Effects Report #5758732-9
Consumer or non-health professional from UNITED STATES reported REBIF problem on June 12, 2007. Male patient, 48 years of age, weighting 187.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: alopecia, central nervous system lesion, fall, hypoaesthesia facial, injection, injection site haemorrhage, injection site pain, injection site reaction, multiple sclerosis relapse, . REBIF dosage: unknown. During the same period patient was treated with AMANTADINE, PROVIGIL, BACLOFEN, DIAZEPAM. Patient was hospitalized. Patient recovered.

Infliximab Side Effects Report #5374435-7
INFLIXIMAB problem was reported by a Health Professional from FINLAND on June 21, 2007. Male patient, 16 years of age, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, central nervous system lesion, cytokine storm, multi-organ failure, pneumonia, post procedural complication, progressive multifocal leukoencephalopathy, sepsis, . INFLIXIMAB dosage: unknown. During the same period patient was treated with AZATHIOPRINE. Patient was hospitalized. Patient died on 04/01/2003.

Carbamazepine Side Effects Report #5297315-4
Physician from JAPAN reported CARBAMAZEPINE problem on Mar 28, 2007. Male patient, 46 years of age, was diagnosed with schizophrenia and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, central nervous system lesion, csf test abnormal, diabetes insipidus, . CARBAMAZEPINE dosage: 600 MG DAILY. During the same period patient was treated with PROMETHAZINE, LITHIUM CARBONATE, NIMETAZEPAM, OXATOMIDE, LISPERIDONE, BULOTIZOLAM. Patient was hospitalized. Patient recovered.

Carbamazepine Side Effects Report #5304661-4
CARBAMAZEPINE problem was reported by a Consumer or non-health professional from JAPAN on Apr 02, 2007. Male patient, 46 years of age, was diagnosed with agitation and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: catatonia, central nervous system lesion, diabetes insipidus, nuclear magnetic resonance imaging brain abnormal, schizophrenia, stupor, . CARBAMAZEPINE dosage: 600 MG QD. During the same period patient was treated with LITHIUM CARBONATE, PROMETHAZINE, FLUNITRAZEPAM, BULOTIZOLAM, NIMETAZEPAM, OXATOMIDE. Patient was hospitalized. Patient recovered.

Nitric Side Effects Report #5273396-9
Physician from SPAIN reported NITRIC OXIDE problem on May 17, 2006. Female patient was diagnosed with lung disorder, prophylaxis and was treated with NITRIC OXIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, central nervous system lesion, hypoxia, intraventricular haemorrhage, necrotising enterocolitis neonatal, neonatal disorder, pneumatosis intestinalis, shock, wound dehiscence, . NITRIC OXIDE dosage: unknown. During the same period patient was treated with NITRIC OXIDE, AMPICILLIN, CEFOTAXIME, AMINOPHYLLIN, INDOMETHACIN, FUROSEMIDE, VANCOMYCIN, FLUCONAZOLE. Patient recovered.

Lipitor Side Effects Report #5618772-7
LIPITOR problem was reported by a Physician from UNITED STATES on Jan 30, 2008. Male patient, weighting 129.0 lb, was diagnosed with blood cholesterol, hyperlipidaemia, back pain and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, central nervous system infection, central nervous system lesion, headache, ill-defined disorder, mobility decreased, nervous system disorder, parasite blood test positive, pyrexia, . LIPITOR dosage: unknown. During the same period patient was treated with LYRICA, PREDNISONE, ACIPHEX, PERCOCET, OLIVE OIL, FISH OIL. Patient recovered.

Lipitor Side Effects Report #5587179-3
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Dec 31, 2007. Male patient, weighting 129.0 lb, was diagnosed with blood cholesterol, back pain and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, central nervous system infection, central nervous system lesion, headache, ill-defined disorder, mobility decreased, nervous system disorder, parasite blood test positive, pyrexia, . LIPITOR dosage: unknown. During the same period patient was treated with LYRICA, PREDNISONE, ACIPHEX, PERCOCET, OLIVE OIL, FISH OIL. Patient recovered.

Neoral Side Effects Report #5515754-0
NEORAL problem was reported by a Consumer or non-health professional from CANADA on Nov 06, 2007. Male patient, 62 years of age, was diagnosed with renal transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, cardiac arrest, central nervous system lesion, chills, confusional state, convulsion, faecal incontinence, heart rate irregular, hypotension, . NEORAL dosage: 200 MG/DAILY. Patient was hospitalized. Patient died on 08/04/2007.

Carbamazepine Side Effects Report #5490616-6
Health Professional from SPAIN reported CARBAMAZEPINE problem on Sept 19, 2007. Female patient, 24 years of age, was diagnosed with partial seizures and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: amnesia, apraxia, central nervous system lesion, dysarthria, motor dysfunction, partial seizures, . CARBAMAZEPINE dosage: 800 MG/DAY. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5500077-6
METHOTREXATE problem was reported by a Consumer or non-health professional from GERMANY on Oct 09, 2007. Male patient, child 7 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: areflexia, arthralgia, central nervous system lesion, dysuria, femur fracture, leukaemia recurrent, meningism, monoparesis, neurotoxicity, . METHOTREXATE dosage: unknown. During the same period patient was treated with CYTARABINE, PREDNISOLONE. Patient recovered.

Carbamazepine Side Effects Report #5369843-4
Consumer or non-health professional from JAPAN reported CARBAMAZEPINE problem on June 05, 2007. Male patient, 46 years of age, was diagnosed with agitation and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, catatonia, central nervous system lesion, diabetes insipidus, nuclear magnetic resonance imaging brain abnormal, stupor, . CARBAMAZEPINE dosage: 600 MG, 1X/DAY:QD. During the same period patient was treated with LITHIUM CARBONATE, PROMETHAZINE, FLUNITRAZEPAM, BULOTIZOLAM, NIMETAZEPAM, OXATAMIDE. Patient was hospitalized. Patient recovered.

Carbamazepine Side Effects Report #5369843-4
CARBAMAZEPINE problem was reported by a Consumer or non-health professional from JAPAN on June 05, 2007. Male patient, 46 years of age, was diagnosed with agitation and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, catatonia, central nervous system lesion, diabetes insipidus, nuclear magnetic resonance imaging brain abnormal, stupor, . CARBAMAZEPINE dosage: 600 MG, 1X/DAY:QD. During the same period patient was treated with LITHIUM CARBONATE, PROMETHAZINE, FLUNITRAZEPAM, BULOTIZOLAM, NIMETAZEPAM, OXATAMIDE. Patient was hospitalized. Patient recovered.

Theophylline Side Effects Report #5775535-X
Physician from JAPAN reported THEOPHYLLINE problem on May 27, 2008. Female patient, 81 years of age, was diagnosed with bronchitis chronic and was treated with THEOPHYLLINE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood creatine phosphokinase increased, central nervous system lesion, complex partial seizures, convulsion, corneal reflex decreased, csf protein increased, encephalopathy, enteritis, . THEOPHYLLINE dosage: 400 MG /D PO. Patient was hospitalized and became disabled. Patient recovered.

Thalidomide Side Effects Report #5798720-X
THALIDOMIDE problem was reported by a Health Professional from UNITED KINGDOM on June 18, 2008. Female patient, 62 years of age, was diagnosed with non-small cell lung cancer and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: amnesia, aphasia, central nervous system lesion, confusional state, disorientation, dysphasia, gait disturbance, hypoaesthesia, lung neoplasm malignant, . THALIDOMIDE dosage: 200 MG, DAILY, ORAL. During the same period patient was treated with GEMCITABINE, CARBOPLATIN, ZOLEDRONIC ACID, DUROGESIC, ORAMORPH. Patient was hospitalized and became disabled. Patient died on 03/20/2006.

Carbamazepine Side Effects Report #5369843-4
Consumer or non-health professional from JAPAN reported CARBAMAZEPINE problem on June 05, 2007. Male patient, 46 years of age, was diagnosed with agitation and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, catatonia, central nervous system lesion, diabetes insipidus, nuclear magnetic resonance imaging brain abnormal, stupor, . CARBAMAZEPINE dosage: 600 MG, 1X/DAY:QD. During the same period patient was treated with LITHIUM CARBONATE, PROMETHAZINE, FLUNITRAZEPAM, BULOTIZOLAM, NIMETAZEPAM, OXATAMIDE. Patient was hospitalized. Patient recovered.