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Iopamiron Side Effects Report #5708589-7
Physician from JAPAN reported IOPAMIRON problem on Apr 09, 2008. Female patient, weighting 92.59 lb, was diagnosed with percutaneous coronary intervention, acute myocardial infarction, arteriogram coronary and was treated with IOPAMIRON. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, clonic convulsion, hemianopia, loss of consciousness, . IOPAMIRON dosage: unknown. During the same period patient was treated with OLIVES K, MYSLEE, ARTIST, PANALDINE, ITOROL, LIPITOR. Patient was hospitalized. Patient recovered.

Sebivo Side Effects Report #5620297-X
SEBIVO problem was reported by a Pharmacist from GERMANY on Jan 29, 2008. Female patient, 52 years of age, weighting 104.7 lb, was diagnosed with hepatitis b and was treated with SEBIVO. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebral atrophy, cerebrovascular disorder, craniotomy, diplopia, nervous system disorder, visual acuity reduced, vith nerve paralysis, . SEBIVO dosage: 600 MG, Q96H. During the same period patient was treated with KELTICAN, RENAGEL, BICARBONATE, CINACALCET, ROCALTROL. Patient recovered.

Tareg Side Effects Report #5635962-8
Consumer or non-health professional from CHILE reported TAREG problem on Feb 18, 2008. Male patient, 70 years of age, was diagnosed with hypertension and was treated with TAREG. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, depressed mood, dizziness, skull fracture, thrombosis, . TAREG dosage: 160 MG, UNK. During the same period patient was treated with ANALGESICS, ANTIEPILEPTICS. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5533391-9
REMICADE problem was reported by a Physician from SPAIN on Nov 23, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebral haemorrhage, hemiplegia, . REMICADE dosage: unknown. Patient recovered.


Hydrocodone Side Effects Report #5534522-7
Consumer or non-health professional from UNITED STATES reported HYDROCODONE BITARTRATE problem on Dec 04, 2007. Male patient, 55 years of age, weighting 220.0 lb, was diagnosed with sensory disturbance and was treated with HYDROCODONE BITARTRATE. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, constipation, dysgeusia, hyperhidrosis, immobile, movement disorder, respiratory depression, somnolence, urticaria, . HYDROCODONE BITARTRATE dosage: unknown. During the same period patient was treated with BACLOFEN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5535084-0
PROGRAF problem was reported by a Pharmacist from UNITED KINGDOM on Nov 15, 2007. Female patient was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, . PROGRAF dosage: unknown. Patient recovered.

Fluorouracil Side Effects Report #5506308-0
Consumer or non-health professional from UNITED STATES reported FLUOROURACIL problem on Nov 02, 2007. Female patient, weighting 170.0 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, carotid artery stenosis, cerebral infarction, neuropathy, peroneal nerve palsy, . FLUOROURACIL dosage: 17472 MG. During the same period patient was treated with BEVACIZUMAB, LEUCOVORIN CALCIUM, ELOXATIN. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5533978-3
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Nov 21, 2007. Female patient, 61 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, convulsion, inflammation, nervous system disorder, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX, CARBAMAZEPINE. Patient was hospitalized. Patient recovered.

Lucentis Side Effects Report #5481298-8
Health Professional from UNITED STATES reported LUCENTIS problem on Oct 05, 2007. Female patient, weighting 220.0 lb, was treated with LUCENTIS. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebral infarction, cerebral ischaemia, cerebral thrombosis, cerebrovascular accident, coagulopathy, gliosis, nuclear magnetic resonance imaging brain abnormal, transient ischaemic attack, . LUCENTIS dosage: 0.5MG ONCE INTRAOCULA. During the same period patient was treated with AVASTIN, OCUVITE, ASPIRIN. Patient was hospitalized. Patient recovered.


Herceptin Side Effects Report #5485912-2
HERCEPTIN problem was reported by a Physician from UNITED KINGDOM on Oct 01, 2007. Female patient, weighting 103.6 lb, was diagnosed with breast cancer and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, depression, suicidal ideation, suicide attempt, . HERCEPTIN dosage: 300 MG, UNK. Patient was hospitalized. Patient recovered.

Temozolomide Side Effects Report #5501714-2
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on Oct 26, 2007. Male patient, weighting 215.2 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, fall, fibrin d dimer increased, musculoskeletal pain, neoplasm progression, pulmonary embolism, . TEMOZOLOMIDE dosage: 2380 MG. During the same period patient was treated with CODEINE SUL, DEXAMETHASONE, ACETAMINOPHEN, PHENYTOIN. Patient was hospitalized. Patient recovered.

Herceptin Side Effects Report #5449395-0
HERCEPTIN problem was reported by a Physician from UNITED KINGDOM on Aug 27, 2007. Female patient, weighting 103.6 lb, was diagnosed with breast cancer and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, depression, suicidal ideation, suicide attempt, . HERCEPTIN dosage: 300 MG, UNK. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5391181-4
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on July 13, 2007. Female patient, 62 years of age, was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebrovascular accident, muscular weakness, . ZELNORM dosage: 10 MG, BID. Patient recovered.

Zelnorm Side Effects Report #5391181-4
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 2007. Female patient, 62 years of age, was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebrovascular accident, muscular weakness, . ZELNORM dosage: 10 MG, BID. Patient recovered.


Sandostatin Side Effects Report #5767818-4
Consumer or non-health professional from CANADA reported SANDOSTATIN LAR problem on June 03, 2008. Female patient was diagnosed with carcinoid tumour, hypertension, hypercholesterolaemia and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, hepatic neoplasm, liver operation, meningioma, road traffic accident, vomiting, . SANDOSTATIN LAR dosage: 20 MG, QMO. During the same period patient was treated with ALTACE, LIPITOR. Patient recovered.

Herceptin Side Effects Report #5743969-5
HERCEPTIN problem was reported by a Physician from UNITED KINGDOM on May 05, 2008. Female patient was diagnosed with breast cancer and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, neuropathy peripheral, . HERCEPTIN dosage: 6 MG/KG, Q3W. Patient recovered.

Zelnorm Side Effects Report #5374355-8
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on June 21, 2007. Female patient, 62 years of age, was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebrovascular accident, muscular weakness, . ZELNORM dosage: 10 MG, BID. Patient recovered.

Avonex Side Effects Report #5375750-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on June 18, 2007. Female patient, 58 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, condition aggravated, diabetes mellitus, fatigue, multiple sclerosis relapse, night sweats, pain, urinary tract infection, . AVONEX dosage: unknown. During the same period patient was treated with GLUCOPHAGE. Patient was hospitalized. Patient recovered.

Ganciclovir Side Effects Report #5330976-X
Physician from ISRAEL reported GANCICLOVIR problem on May 15, 2007. Male patient, 70 years of age, weighting 147.7 lb, was diagnosed with glioma and was treated with GANCICLOVIR. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cardiac arrest, pneumonia aspiration, respiratory distress, respiratory failure, . GANCICLOVIR dosage: unknown. During the same period patient was treated with CEREPRO, PHENYTOIN, RANITIDINE, HEPARIN, LACTULOSE, AMLODIPINE, CEFTAZIDIME, VANCOMYCIN. Patient died on 09/28/2006.


Irinotecan Side Effects Report #5343890-0
IRINOTECAN problem was reported by a Consumer or non-health professional from UNITED STATES on May 31, 2007. Male patient, weighting 185.2 lb, was diagnosed with glioblastoma multiforme and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, diarrhoea, nausea, neoplasm progression, oedema, somnolence, unresponsive to stimuli, . IRINOTECAN dosage: 325MG/M2 DAY 1, 8, 22, 29 IV. During the same period patient was treated with TEMODAR, DEXAMETHASONE, ZANTAC, PHENOBARBITAL. Patient was hospitalized. Patient recovered.

Mabthera Side Effects Report #5291373-9
Physician from SWEDEN reported MABTHERA problem on Mar 22, 2007. Male patient, 65 years of age, was diagnosed with rheumatoid arthritis and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, facial palsy, monoparesis, muscular weakness, scar, speech disorder, . MABTHERA dosage: unknown. During the same period patient was treated with SELOKEN ZOC, METHOTREXATE, PRAVACHOL, CONFORTID, ASPIRIN, ACETYLCYSTEINE. Patient was hospitalized. Patient recovered.

Alka Side Effects Report #5308001-6
ALKA SELTZER PLUS problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2007. Female patient, weighting 119.0 lb, was diagnosed with nasal congestion and was treated with ALKA SELTZER PLUS. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, . ALKA SELTZER PLUS dosage: unknown. During the same period patient was treated with ALKA SELTZER PLUS FLU, ALKA SELTZER PLUS DAY, ALKA SELTZER PLUS NIGHT. Patient recovered.

Vivelle Side Effects Report #5339088-2
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Feb 27, 2006. Male patient, 81 years of age, was diagnosed with prostate cancer and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebrovascular accident, prescribed overdose, prostatic specific antigen increased, visual disturbance, . VIVELLE dosage: unknown. During the same period patient was treated with KETOCONAZOLE, ESTRADIOL, AVODART, LEUKINE. Patient recovered.

Alka Side Effects Report #5262209-7
ALKA SELTZER PLUS problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Female patient, weighting 119.0 lb, was diagnosed with nasal congestion and was treated with ALKA SELTZER PLUS. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, . ALKA SELTZER PLUS dosage: unknown. During the same period patient was treated with ALKA SELTZER PLUS FLU, ALKA SELTZER PLUS DAY, ALKA SELTZER PLUS NIGHT. Patient recovered.

Bevacizumab Side Effects Report #5279577-2
Physician from UNITED STATES reported BEVACIZUMAB problem on Mar 12, 2007. Male patient, 68 years of age, weighting 160.7 lb, was diagnosed with non-small cell lung cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: brain scan abnormal, cerebral arteriosclerosis, condition aggravated, depressed level of consciousness, fall, leukoencephalopathy, . BEVACIZUMAB dosage: unknown. During the same period patient was treated with DOCETAXEL, LOVASTATIN, ATENOLOL, CARBOPLATIN, LISINOPRIL, ASPIRIN, LANTUS, HUMALOG. Patient was hospitalized. Patient recovered.

Memantine Side Effects Report #5650223-9
MEMANTINE problem was reported by a Health Professional from FRANCE on Feb 12, 2008. Male patient, 77 years of age, was treated with MEMANTINE. After drug was administered, patient experienced the following problems/side effects: aspiration, brain scan abnormal, cerebral atrophy, coma, convulsion, depressed level of consciousness, disorientation, dyskinesia, electrocardiogram abnormal, . MEMANTINE dosage: 20 MG QD;PO. During the same period patient was treated with MIRTAZAPINE, MEPROBAMATE, MODOPAR, THEOSTAT, ZOCOR, PLAVIX. Patient was hospitalized. Patient died on 11/08/2007.

Zometa Side Effects Report #5585337-5
Health Professional from UNITED STATES reported ZOMETA problem on Jan 04, 2008. Male patient, 53 years of age, weighting 220.5 lb, was diagnosed with osteoporosis and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: aphasia, brain scan abnormal, constipation, dysarthria, facial palsy, faecal incontinence, feeling hot, induration, infection, . ZOMETA dosage: 4MG Q 90 DAYS IV. During the same period patient was treated with KEPPRA, DEXAMETHASONE, TRILEPTAL, ZANTAC, MINOCYCLINE, RESTORIL. Patient was hospitalized. Patient recovered.

Bleomycin Side Effects Report #5533945-X
BLEOMYCIN problem was reported by a Physician from CANADA on Nov 20, 2007. Male patient, child 9 years of age, was diagnosed with craniopharyngioma and was treated with BLEOMYCIN. After drug was administered, patient experienced the following problems/side effects: brain oedema, brain scan abnormal, diabetes insipidus, fatigue, hypothalamo-pituitary disorder, injection site extravasation, memory impairment, scar, temperature intolerance, . BLEOMYCIN dosage: 3 MG 3/WK OTHER. During the same period patient was treated with CHLORIDE. Patient was hospitalized. Patient recovered.

Saizen Side Effects Report #5495518-7
Physician from FRANCE reported SAIZEN problem on Oct 08, 2007. Male patient, 37 years of age, was diagnosed with hypopituitarism and was treated with SAIZEN. After drug was administered, patient experienced the following problems/side effects: balance disorder, brain scan abnormal, condition aggravated, fall, vertigo, . SAIZEN dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, CYNOMEL, HYDROCORTISONE, DEPAKENE, LAMICTAL. Patient was hospitalized. Patient recovered.

Olmesartan Side Effects Report #5451029-6
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE problem was reported by a Health Professional from FRANCE on Aug 31, 2007. Female patient, 83 years of age, weighting 154.3 lb, was diagnosed with hypertension and was treated with OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, brain scan abnormal, bronchitis, fall, hypercalcaemia, incontinence, malaise, transient ischaemic attack, vitamin d decreased, . OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE dosage: 20/25MG (ONCE A DAY), ORAL. During the same period patient was treated with ATENOLOL, ACETYL, SERETIDE, CARBOCYSTEINE, TRIAMCINOLONE, LYSINE ACETYLSALICYLATE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Rabeprazole Side Effects Report #5472537-8
Physician from ITALY reported RABEPRAZOLE problem on Sept 14, 2007. Female patient, 74 years of age, was diagnosed with ulcer, dyslipidaemia and was treated with RABEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: amnesia, brain scan abnormal, confusional state, dyslexia, gait disturbance, movement disorder, tremor, . RABEPRAZOLE dosage: 10 MG,. During the same period patient was treated with ATORVASTATIN CALCIUM, CLOPIDOGREL, ACETYLSALICYLIC ACID SRT, RAMIPRIL, SALMETEROL, CLEBOPRIDE. Patient was hospitalized. Patient recovered.

Tyzeka Side Effects Report #5427079-2
TYZEKA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2007. Male patient was diagnosed with prophylaxis and was treated with TYZEKA. After drug was administered, patient experienced the following problems/side effects: brain damage, brain scan abnormal, cyanosis neonatal, infantile apnoeic attack, . TYZEKA dosage: unknown. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5759315-7
Physician from POLAND reported PROGRAF problem on May 16, 2008. Female patient, 53 years of age, weighting 145.5 lb, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, brain scan abnormal, bronchopulmonary aspergillosis, convulsion, infection, loss of consciousness, septic shock, speech disorder, transplant rejection, . PROGRAF dosage: 3 MG, BID, ORAL. During the same period patient was treated with ENCORTON, URSO, METOCARD, AMLOZEK, PIPERACILLIN AND TAZOBACTAM, DIFLUCAN, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5733158-2
PROGRAF problem was reported by a Physician from POLAND on Apr 22, 2008. Female patient, 53 years of age, weighting 145.5 lb, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, brain scan abnormal, bronchopulmonary aspergillosis, convulsion, infection in an immunocompromised host, neurological symptom, transplant rejection, tremor, . PROGRAF dosage: 7 MG, UID/QD, ORAL. During the same period patient was treated with ENCORTON, URSO, METOCARD, AMLOZEK, TAZOCIN, DIFLUCAN. Patient died on 04/11/2008.

Duragesic Side Effects Report #5744964-2
Physician from GERMANY reported DURAGESIC problem on May 13, 2008. Male patient, 70 years of age, was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: agitation, brain scan abnormal, coma, hallucination, overdose, . DURAGESIC dosage: unknown. During the same period patient was treated with MUSARIL, BECLAMETHASONE, EUNERPAN, NEXIUM, CORTISONE. Patient was hospitalized. Patient recovered.

Ixabepilone Side Effects Report #5719622-0
IXABEPILONE problem was reported by a Consumer or non-health professional from FRANCE on Apr 22, 2008. Female patient, 33 years of age, weighting 200.6 lb, was diagnosed with breast cancer and was treated with IXABEPILONE. After drug was administered, patient experienced the following problems/side effects: asthenia, brain scan abnormal, constipation, diarrhoea, dizziness, febrile neutropenia, oral fungal infection, . IXABEPILONE dosage: CUMULATIVE DOSE SINCE FIRST ADMINISTRATION: 100 MG. During the same period patient was treated with ENDOXAN, EPIRUBICIN, FLUOROURACIL, NEULASTA, GRANOCYTE. Patient was hospitalized. Patient recovered.

Isotretinoin Side Effects Report #5343562-2
Health Professional from FRANCE reported ISOTRETINOIN problem on May 16, 2007. Male patient, 30 years of age, was diagnosed with acne and was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: aphasia, brain scan abnormal, cerebral ischaemia, dysarthria, facial palsy, . ISOTRETINOIN dosage: 45 MG, QD, ORAL. Patient recovered.

Temodar Side Effects Report #5650057-5
TEMODAR problem was reported by a Health Professional from UNITED STATES on Feb 19, 2008. Female patient, 57 years of age, was diagnosed with gliosarcoma and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood pressure inadequately controlled, brain scan abnormal, contusion, epistaxis, fall, haematemesis, haemorrhage intracranial, hemiparesis, . TEMODAR dosage: 125 MG; QD; PO; 300 MG;. During the same period patient was treated with DECADRON, LEXAPRO, PHENYTOIN. Patient was hospitalized and became disabled. Patient died on 01/06/2008.

Prozac Side Effects Report #5545610-3
Consumer or non-health professional from UNITED KINGDOM reported PROZAC problem on Nov 28, 2007. Male patient, 32 years of age, was treated with PROZAC. After drug was administered, patient experienced the following problems/side effects: alcoholism, brain damage, brain scan abnormal, cerebrovascular accident, confusional state, memory impairment, road traffic accident, speech disorder, suicidal ideation, . PROZAC dosage: unknown. Patient was hospitalized. Patient recovered.

Decitabine Side Effects Report #5506432-2
DECITABINE problem was reported by a Physician from TURKEY on Oct 22, 2007. Female patient, 64 years of age, weighting 163.1 lb, was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, blood fibrinogen abnormal, brain scan abnormal, caecitis, diarrhoea, disease progression, fibrin d dimer increased, haemoglobin decreased, haemorrhage intracranial, . DECITABINE dosage: 225 MG, INTRAVENOUS. Patient was hospitalized and became disabled. Patient died on 03/22/2007.

Baclofen Side Effects Report #5524716-9
Consumer or non-health professional from SLOVENIA reported BACLOFEN problem on Nov 13, 2007. Male patient, 60 years of age, weighting 163.1 lb, was diagnosed with diabetes mellitus and was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: anuria, blood creatinine increased, brain scan abnormal, coma, creatinine renal clearance decreased, depressed level of consciousness, dyspnoea, glasgow coma scale abnormal, . BACLOFEN dosage: 25 MG, Q12H. During the same period patient was treated with INSULIN. Patient was hospitalized. Patient recovered.

Baclofen Side Effects Report #5448270-5
BACLOFEN problem was reported by a Health Professional from SLOVENIA on Sept 04, 2007. Male patient, 60 years of age, weighting 163.1 lb, was diagnosed with diabetes mellitus and was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: anuria, blood creatinine increased, brain scan abnormal, coma, creatinine renal clearance decreased, depressed level of consciousness, dyspnoea, glasgow coma scale abnormal, . BACLOFEN dosage: 25 MG, Q12H. During the same period patient was treated with INSULIN. Patient was hospitalized. Patient recovered.

Etomidate Side Effects Report #5796744-X
Physician from UNITED STATES reported ETOMIDATE problem on June 16, 2008. Male patient, 61 years of age, was diagnosed with subarachnoid haemorrhage and was treated with ETOMIDATE. After drug was administered, patient experienced the following problems/side effects: apnoea, atrial fibrillation, brain scan abnormal, cerebral infarction, loss of consciousness, renal failure, toxic epidermal necrolysis, . ETOMIDATE dosage: unknown. Patient was hospitalized. Patient died.

Femara Side Effects Report #5754094-1
FEMARA problem was reported by a Consumer or non-health professional from FRANCE on May 26, 2008. Female patient was diagnosed with breast cancer and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: amnesia, brain oedema, brain scan abnormal, cerebral haematoma, coma, glasgow coma scale abnormal, international normalised ratio increased, . FEMARA dosage: 2.5 MG, QD. During the same period patient was treated with COUMADIN, VASTAREL, AMITRIPTYLINE, DAFLON. Patient was hospitalized. Patient died on 04/24/2008.

Norditropin Side Effects Report #5691533-9
Physician from FRANCE reported NORDITROPIN problem on Dec 19, 2006. Male patient, 23 years of age, weighting 165.3 lb, was diagnosed with growth hormone deficiency, diabetes insipidus, blood luteinising hormone abnormal and was treated with NORDITROPIN. After drug was administered, patient experienced the following problems/side effects: anorexia, asthenia, brain scan abnormal, electroencephalogram abnormal, epilepsy, pallor, somnolence, weight decreased, . NORDITROPIN dosage: .3 MG, QD. During the same period patient was treated with LEVOTHYROXINE, HYDROCORTISONE, MINRIN, ANDROTARDYL. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5368913-4
METHOTREXATE PRESERVATIVE FREE problem was reported by a Pharmacist from UNITED STATES on June 21, 2007. Male patient, weighting 110.2 lb, was diagnosed with acute lymphocytic leukaemia and was treated with METHOTREXATE PRESERVATIVE FREE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, anxiety, brain scan abnormal, confusional state, delirium, demyelination, electroencephalogram abnormal, epilepsy, flight of ideas, . METHOTREXATE PRESERVATIVE FREE dosage: 15 MG X3 IT. Patient was hospitalized. Patient recovered.

Exenatide Side Effects Report #5370122-X
Physician from UNITED STATES reported EXENATIDE problem on June 11, 2007. Female patient, 43 years of age, was diagnosed with diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: anorexia, brain mass, brain scan abnormal, computerised tomogram, hyperglycaemia, hypernatraemia, mental impairment, mental status changes, . EXENATIDE dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, DDAVP, PREDNISONE, INSULIN GLARGINE. Patient was hospitalized. Patient recovered.