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Lamictal Side Effects Report #5636820-5
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Feb 20, 2008. Female patient, 14 years of age, weighting 101.0 lb, was diagnosed with bipolar disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: aphagia, thermal burn, visual disturbance, . LAMICTAL dosage: 25 MG DAILY PO. Patient was hospitalized and became disabled. Patient recovered.

Temodal Side Effects Report #5643080-8
TEMODAL problem was reported by a Physician from JAPAN on Feb 18, 2008. Male patient, 38 years of age, weighting 119.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: aphagia, disease progression, glioblastoma multiforme, hepatic function abnormal, herpes virus infection, nausea, vomiting, . TEMODAL dosage: 150 MG/M2; QD; PO. During the same period patient was treated with NASEA, WAKOBITAL, BETAMETHASONE, GLYCEOL. Patient was hospitalized. Patient died on 03/17/2007.

Citalopram Side Effects Report #5648741-2
Consumer or non-health professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on Feb 13, 2008. Female patient, 54 years of age, weighting 145.5 lb, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: aphagia, dizziness, hyperhidrosis, syncope, syncope vasovagal, tachycardia, . CITALOPRAM HYDROBROMIDE dosage: 20 MG QD PO. During the same period patient was treated with CANNABIS. Patient was hospitalized. Patient recovered.

Permax Side Effects Report #5584487-7
PERMAX problem was reported by a Physician from JAPAN on Apr 19, 2007. Male patient, 73 years of age, was diagnosed with parkinson's disease and was treated with PERMAX. After drug was administered, patient experienced the following problems/side effects: aphagia, pericardial effusion, pericarditis, pleural effusion, . PERMAX dosage: unknown. During the same period patient was treated with MENESIT, PARMIPEXOLE, PROSTAL, HARNAL, MAGNESIUM OXIDE, MUCODYNE, MUCOSAL, AMBROXOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.


Keppra Side Effects Report #5606902-2
Consumer or non-health professional from UNITED STATES reported KEPPRA problem on Jan 10, 2008. Male patient, 78 years of age, was diagnosed with traumatic brain injury and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: aphagia, fatigue, miosis, somnolence, tremor, . KEPPRA dosage: unknown. During the same period patient was treated with ZYPREXA, NAMENDA, ARICEPT. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5562498-5
BOTOX problem was reported by a Physician from UNITED STATES on Dec 07, 2007. Female patient was diagnosed with torticollis and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: aphagia, breast cancer recurrent, dysphagia, . BOTOX dosage: unknown. During the same period patient was treated with COGENTIN, CLONAZEPAM, PREVACID. Patient recovered.

Geodon Side Effects Report #5580166-0
Pharmacist from UNITED STATES reported GEODON problem on Dec 27, 2007. Male patient, 41 years of age, was diagnosed with bipolar disorder and was treated with GEODON. After drug was administered, patient experienced the following problems/side effects: aphagia, oral disorder, . GEODON dosage: unknown. Patient recovered.

Natalizumab Side Effects Report #5442862-5
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Aug 22, 2007. Male patient, 57 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: aphagia, asthenia, dysstasia, facial palsy, pneumonia aspiration, respiratory failure, upper respiratory tract infection, urinary retention, white blood cell count decreased, . NATALIZUMAB dosage: 300 MG;QM; IV. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5388758-9
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem on June 27, 2007. Female patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: aphagia, cystitis, hypotension, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.


Revlimid Side Effects Report #5388876-5
REVLIMID problem was reported by a Physician from UNITED STATES on July 06, 2007. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: aphagia, asthenia, dehydration, dizziness, stomatitis, . REVLIMID dosage: 25 MG, QD X 21 DAYS THEN 7 OFF, ORAL. During the same period patient was treated with DUONEB, DRUAGESIC, PERCOCET, ATENOLOL, LASIX, PLAVIX, PROTONIX, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5388758-9
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem on June 27, 2007. Female patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: aphagia, cystitis, hypotension, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5388876-5
REVLIMID problem was reported by a Physician from UNITED STATES on July 06, 2007. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: aphagia, asthenia, dehydration, dizziness, stomatitis, . REVLIMID dosage: 25 MG, QD X 21 DAYS THEN 7 OFF, ORAL. During the same period patient was treated with DUONEB, DRUAGESIC, PERCOCET, ATENOLOL, LASIX, PLAVIX, PROTONIX, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5760846-4
Consumer or non-health professional from UNITED STATES reported BONIVA problem on May 28, 2008. Female patient was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: aphagia, auricular swelling, constipation, insomnia, lip swelling, micturition frequency decreased, oesophageal oedema, pharyngeal oedema, . BONIVA dosage: unknown. Patient recovered.

Boniva Side Effects Report #5788749-X
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 18, 2008. Female patient was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: aphagia, auricular swelling, constipation, insomnia, lip swelling, micturition frequency decreased, oesophageal oedema, pharyngeal oedema, . BONIVA dosage: unknown. Patient recovered.


Boniva Side Effects Report #5731780-0
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Apr 28, 2008. Female patient, 52 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: aphagia, constipation, insomnia, micturition frequency decreased, oesophageal oedema, . BONIVA dosage: unknown. Patient recovered.

Dysport Side Effects Report #5707698-6
DYSPORT problem was reported by a Physician from NETHERLANDS on Apr 07, 2008. Female patient was diagnosed with salivary hypersecretion, amyotrophic lateral sclerosis and was treated with DYSPORT. After drug was administered, patient experienced the following problems/side effects: aphagia, cranial nerve disorder, dysarthria, lung disorder, palatal disorder, paresis, . DYSPORT dosage: unknown. Patient died.

Boniva Side Effects Report #5717649-6
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Apr 17, 2008. Female patient, 52 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: aphagia, constipation, insomnia, micturition frequency decreased, oesophageal oedema, . BONIVA dosage: unknown. Patient recovered.

Cisplatin Side Effects Report #5371683-7
CISPLATIN problem was reported by a Consumer or non-health professional from SPAIN on June 13, 2007. Male patient, 72 years of age, weighting 132.3 lb, was diagnosed with hypopharyngeal cancer and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: aphagia, catheter related complication, mucosal inflammation, septic phlebitis, staphylococcal bacteraemia, . CISPLATIN dosage: 170 MG IV. During the same period patient was treated with FLUOROURACIL, FLUIMUCIL, PARACETAMOL, NEOBRUFEN, DURAGESIC, ACTOS. Patient was hospitalized. Patient recovered.

Fabrazyme Side Effects Report #5372687-0
Physician from COLOMBIA reported FABRAZYME problem on Apr 28, 2007. Male patient, 53 years of age, weighting 154.3 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: aphagia, cardio-respiratory arrest, catheter related infection, cerebral ischaemia, dialysis device complication, infusion site infection, loss of consciousness, neurological symptom, peritonitis, . FABRAZYME dosage: 70 MG QW2KS IV. During the same period patient was treated with METOPROLOL SUCCINATE, CALCIUM CHLORIDE, OMEPRAZOLE, EPOGEN. Patient was hospitalized. Patient died on 09/02/2006.


Miacalcin Side Effects Report #5317616-0
MIACALCIN problem was reported by a Consumer or non-health professional from CANADA on Apr 26, 2007. Male patient, 83 years of age, was diagnosed with osteoporosis and was treated with MIACALCIN. After drug was administered, patient experienced the following problems/side effects: aphagia, hemiplegia, transient ischaemic attack, visual disturbance, . MIACALCIN dosage: unknown. During the same period patient was treated with CALCIUM CHLORIDE, OMEPRAZOLE, VENTOLIN, BRICANYL, PREDNISONE, VITAMIN D. Patient was hospitalized. Patient recovered.

Rilutek Side Effects Report #5329945-5
Consumer or non-health professional from UNITED STATES reported RILUTEK problem on May 17, 2007. Male patient, 75 years of age, was diagnosed with amyotrophic lateral sclerosis and was treated with RILUTEK. After drug was administered, patient experienced the following problems/side effects: aphagia, dyspnoea, . RILUTEK dosage: unknown. Patient was hospitalized. Patient died on 10/22/2006.

Avandaryl Side Effects Report #5338695-0
AVANDARYL problem was reported by a Consumer or non-health professional from UNITED STATES on May 25, 2007. Male patient, 63 years of age, was treated with AVANDARYL. After drug was administered, patient experienced the following problems/side effects: aphagia, blood glucose decreased, facial paresis, headache, . AVANDARYL dosage: unknown. Patient recovered.

Dexamethasone Side Effects Report #5340024-3
Consumer or non-health professional from UNITED KINGDOM reported DEXAMETHASONE problem on May 22, 2007. Male patient, 76 years of age, was diagnosed with brain neoplasm and was treated with DEXAMETHASONE. After drug was administered, patient experienced the following problems/side effects: aphagia, oesophageal candidiasis, reflux oesophagitis, . DEXAMETHASONE dosage: 4 MG QD ORAL. Patient recovered.

Rebif Side Effects Report #5309158-3
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 12, 2007. Female patient, 39 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: aphagia, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Fabrazyme Side Effects Report #5256004-2
Physician from COLOMBIA reported FABRAZYME problem on Feb 15, 2007. Male patient, 53 years of age, weighting 154.3 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: aphagia, cardio-respiratory arrest, catheter related infection, cerebral ischaemia, dialysis device complication, infusion site infection, loss of consciousness, peritonitis, sepsis, . FABRAZYME dosage: 70 MG Q2WKS IV. During the same period patient was treated with METOPROLOL SUCCINATE, CALCIUM, OMEPRAZOLE, EPOGEN. Patient was hospitalized. Patient died on 09/02/2006.

Solodyn Side Effects Report #5273241-1
SOLODYN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2007. Male patient, 22 years of age, weighting 204.0 lb, was diagnosed with acne and was treated with SOLODYN. After drug was administered, patient experienced the following problems/side effects: aphagia, eye swelling, gastrooesophageal reflux disease, odynophagia, pharyngeal oedema, productive cough, rash, vomiting, . SOLODYN dosage: unknown. Patient recovered.

Tildiem Side Effects Report #5273342-8
Pharmacist from UNITED KINGDOM reported TILDIEM problem on Mar 02, 2007. Female patient was treated with TILDIEM. After drug was administered, patient experienced the following problems/side effects: aphagia, . TILDIEM dosage: unknown. During the same period patient was treated with TRITACE. Patient recovered.

Miacalcin Side Effects Report #5274101-2
MIACALCIN problem was reported by a Consumer or non-health professional from CANADA on Mar 13, 2007. Male patient, 83 years of age, was diagnosed with osteoporosis and was treated with MIACALCIN. After drug was administered, patient experienced the following problems/side effects: aphagia, hemiplegia, visual disturbance, . MIACALCIN dosage: unknown. Patient recovered.

Chantix Side Effects Report #5513310-1
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Oct 31, 2007. Male patient, weighting 175.4 lb, was diagnosed with hypertension and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, aphagia, blister, mouth ulceration, . CHANTIX dosage: unknown. During the same period patient was treated with ZESTORETIC, VITAMIN CAP, ASPIRIN, GLUCOSAMINE SULPHATE. Patient recovered.

Chantix Side Effects Report #5528289-6
CHANTIX problem was reported by a Health Professional from UNITED STATES on Nov 16, 2007. Female patient, weighting 210.4 lb, was diagnosed with ex-smoker, dyspnoea, atrial fibrillation, bronchitis and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: abdominal distension, aphagia, asthenia, bronchitis, contusion, dyspnoea, fatigue, haemoglobin decreased, haemorrhage, . CHANTIX dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE SUCCINATE, PREDNISONE, WARFARIN, LEVAQUIN, TOPROL, CELEBREX, SPIRIVA. Patient was hospitalized and became disabled. Patient recovered.

Seroquel Side Effects Report #5739784-9
Consumer or non-health professional from UNITED STATES reported SEROQUEL problem on May 12, 2008. Female patient, weighting 120.0 lb, was diagnosed with dementia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: aggression, aphagia, confusional state, dystonia, pain, psychotic disorder, skin discolouration, . SEROQUEL dosage: unknown. During the same period patient was treated with HALDOL. Patient was hospitalized. Patient recovered.

Crest Side Effects Report #5369438-2
CREST W problem was reported by a Physician from UNITED STATES on Mar 22, 2007. Female patient, 87 years of age, weighting 147.9 lb, was treated with CREST W. After drug was administered, patient experienced the following problems/side effects: angioedema, aphagia, aphasia, blood pressure increased, choking sensation, dysphonia, glossodynia, heart rate increased, . CREST W dosage: unknown. During the same period patient was treated with CREST W, ANTIHYPERTENSIVES, DIURETICS, POTASSIUM, PREMARIN, FUROSEMIDE, OXYBUTYNIN CHLORIDE, NIFEDICAL. Patient recovered.

Temozolomide Side Effects Report #5257049-9
Physician from UNITED STATES reported TEMOZOLOMIDE problem on Feb 26, 2007. Female patient, 74 years of age, weighting 135.1 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: anorexia, aphagia, atelectasis, cognitive disorder, disease progression, haemoglobin decreased, hemiparesis, herpes zoster, . TEMOZOLOMIDE dosage: 125 MG;QD;PO. During the same period patient was treated with RADIATION, ZIAC, PROTONIX, AVANDIA, PRANDIN, PHENYTOIN, BACTRIM, XOPENEX. Patient was hospitalized. Patient died on 02/12/2007.

Zyvox Side Effects Report #5283301-7
ZYVOX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 28, 2007. Male patient, weighting 164.0 lb, was diagnosed with staphylococcal infection and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: ageusia, aphagia, asthenia, diarrhoea, . ZYVOX dosage: 600 MG TWICE DAILY BY MOUTH. Patient recovered.

Temozolomide Side Effects Report #5765308-6
Health Professional from UNITED STATES reported TEMOZOLOMIDE problem on June 09, 2008. Female patient, 59 years of age, weighting 113.8 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: agitation, anxiety, aphagia, arthralgia, back pain, confusional state, constipation, hypokalaemia, . TEMOZOLOMIDE dosage: 300 MG DAY 1 TO 5 PO. During the same period patient was treated with VELCADE, LACTULOSE, NEXIUM, MORPHINE CADD PUMP, ATIVAN, LASIX, COLACE. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5701396-0
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 02, 2008. Male patient, 83 years of age, weighting 169.8 lb, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: abasia, ageusia, aphagia, aphasia, asthenia, blood pressure decreased, cerebrovascular accident, decreased appetite, . HEPARIN dosage: unknown. During the same period patient was treated with CRESTOR, TRICOR, CALCITRIOL, VITAMIN A, AMICOR FISH S, DIANEAL, VENOFER. Patient was hospitalized. Patient died on 03/06/2008.

Lamictal Side Effects Report #5266683-1
Consumer or non-health professional from NEW ZEALAND reported LAMICTAL problem on Feb 26, 2007. Male patient, child 12 years of age, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: aphagia, disturbance in social behaviour, grand mal convulsion, haematemesis, legal problem, . LAMICTAL dosage: unknown. During the same period patient was treated with LORAZEPAM, PHENYTOIN. Patient was hospitalized. Patient recovered.