MYSOLINE Side Effects

6926424-6 | Abdominal Pain, Asthma, Bile Duct Stone, Cholelithiasis, Decreased Appetite, Energy Increased, Enzyme Abnormality, Hiatus Hernia
on Aug 05, 2010 Female patient from UNITED STATES , weighting 144.0 lb, was diagnosed with grand mal convulsion and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), asthma (What is asthma?), bile duct stone, cholelithiasis, decreased appetite, energy increased, enzyme abnormality, hiatus hernia. Mysoline dosage: 1 Yellow Tablet, Tid. Patient was hospitalized.

6718517-3 |
Patient was taking Mysoline (View Usage). on Apr 28, 2010 from UNITED STATES Additional patient health information: Female patient , 63 years of age, . Mysoline dosage: Unk.

6663207-9 | Condition Aggravated, Tremor
Adverse event was reported on Mar 30, 2010 by a Female patient taking Mysoline (View Usage) (Dosage: One Am One Hs) was diagnosed with tremor and. Location: UNITED STATES , weighting 152.0 lb, After Mysoline was administered, patient had the following side effects: condition aggravated, tremor.

6557856-6 | Product Substitution Issue
on Jan 28, 2010 Female patient from UNITED STATES , 53 years of age, was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: product substitution issue. Mysoline dosage: . During the same period patient was treated with DILANTIN (View Dilantin Review and Dilantin Label ).


6540126-X | Abdominal Pain, Bile Duct Stone, Cholelithiasis, Decreased Appetite, Enzyme Abnormality, Hiatus Hernia, Lethargy, Nausea
on Jan 05, 2010 Female patient from UNITED STATES , weighting 144.0 lb, was diagnosed with grand mal convulsion and was treated with Mysoline (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), bile duct stone, cholelithiasis, decreased appetite, enzyme abnormality, hiatus hernia, lethargy, nausea (What is nausea?). Mysoline dosage: 1 Yellow Tablet, Tid. Patient was hospitalized.

6524166-2 | Abdominal Pain, Bile Duct Stone, Cholelithiasis, Decreased Appetite, Enzyme Abnormality, Hiatus Hernia, Lethargy, Nausea
Patient was taking Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), bile duct stone, cholelithiasis, decreased appetite, enzyme abnormality, hiatus hernia, lethargy, nausea (What is nausea?) on Dec 18, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 144.0 lb, was diagnosed with grand mal convulsion and. Mysoline dosage: 1 Yellow Tablet, Tid. Patient was hospitalized.

6400776-8 | Convulsion, Fall, Skin Laceration
Adverse event was reported on Oct 02, 2009 by a Male patient taking Mysoline (View Usage) (Dosage: 250 Mg, 1 Tid And 2 Qhs) was diagnosed with epilepsy (What is epilepsy?), convulsion and. Location: UNITED STATES , weighting 244.7 lb, Patient experienced the following unwanted or unexpected effects: convulsion, fall (What is fall?), skin laceration. During the same period patient was treated with TEGRETOL (View Tegretol Review and Tegretol Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), TRIAMTERENE AND HYDROCHLOROTHIAZIDE (View Triamterene And Hydrochlorothiazide Review and Triamterene And Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

6317476-5 | Cough, Dysphagia, Product Quality Issue, Throat Irritation
on Aug 20, 2009 Female patient from UNITED STATES , 57 years of age, weighting 95.00 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). Patient had the following side effects: cough, dysphagia, product quality issue, throat irritation. Mysoline dosage: 250 Mg 4 Daily Every 6 Hrs New Tablet First Taken.

6265529-2 | Hypoaesthesia
on Jul 09, 2009 Male patient from UNITED STATES , 57 years of age, weighting 180.0 lb, was diagnosed with epilepsy (What is epilepsy?) and was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: hypoaesthesia. Mysoline dosage: Half Twice Per Day Po.

6232105-7 | Blood Pressure Increased, Contusion, Fall, Head Injury, Periorbital Haematoma, Skin Laceration
Patient was taking Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, contusion, fall (What is fall?), head injury, periorbital haematoma, skin laceration on Jun 05, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 103.0 lb, was diagnosed with convulsion, tremor and. Mysoline dosage: 250 Mg, Tid. During the same period patient was treated with XANAX (0.5 Mg, Qid) (View Xanax Review and Xanax Label ), SUMATRIPTAN SUCCINATE (Unk) (View Sumatriptan Succinate Review and Sumatriptan Succinate Label ), FOSAMAX (Unk) (View Fosamax Review and Fosamax Label ). Patient was hospitalized.

6150243-4 | Confusional State, Dizziness, Nausea
Adverse event was reported on Apr 07, 2009 by a Female patient taking Mysoline (View Usage) (Dosage: 50 Mgm Hs Po) was diagnosed with tremor and. Location: UNITED STATES , weighting 120.0 lb, Patient had the following side effects: confusional state, dizziness (What is dizziness?), nausea (What is nausea?).

5958265-0 | Convulsion, Energy Increased, Fatigue
on Oct 31, 2008 Female patient from UNITED STATES , weighting 108.0 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: convulsion, energy increased, fatigue. Mysoline dosage: 125 Mg Tid Oral. During the same period patient was treated with DILANTIN (Df Oral) (View Dilantin Review and Dilantin Label ), VALIUM (View Valium Review and Valium Label ), MEBARAL (View Mebaral Review and Mebaral Label ).

5955946-X | Completed Suicide, Homicide
on Oct 27, 2008 Male patient from UNITED STATES , weighting 160.0 lb, was diagnosed with parkinson's disease (What is parkinson's disease?) and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: completed suicide, homicide. Mysoline dosage: (25 Mg Qd Oral), (50 Mg Qd Oral). During the same period patient was treated with COREG (View Coreg Review and Coreg Label ).

5941879-1 | Product Quality Issue, Visual Impairment
Patient was taking Mysoline (View Usage). Patient had the following side effects: product quality issue, visual impairment on Nov 04, 2008 from UNITED STATES Additional patient health information: Female patient , 69 years of age, weighting 100.0 lb, was diagnosed with epilepsy (What is epilepsy?) and. Mysoline dosage: 1 Tablet Twice Daily Po. During the same period patient was treated with DILANTIN (View Dilantin Review and Dilantin Label ).

5877479-1 | Convulsion
Adverse event was reported on Aug 22, 2008 by a Female patient taking Mysoline (View Usage) (Dosage: (250 Mg Tid Oral), (250 Mg Tid Oral)) was diagnosed with convulsion and. Location: UNITED STATES , weighting 104.0 lb, After Mysoline was administered, patient had the following side effects: convulsion. During the same period patient was treated with DILANTIN (View Dilantin Review and Dilantin Label ), VALIUM (View Valium Review and Valium Label ).

5876855-0 | Dizziness, Mental Impairment, Pruritus, Thinking Abnormal, Vision Blurred
on Aug 22, 2008 Female patient from UNITED STATES , 81 years of age, weighting 145.0 lb, was diagnosed with epilepsy (What is epilepsy?) and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), mental impairment, pruritus, thinking abnormal, vision blurred. Mysoline dosage: 50 Mg 8x/day Oral), (50 Mg Bid Oral). During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), VASOTEC (View Vasotec Review and Vasotec Label ).

5875692-0 | Convulsion, Malaise, Migraine
on Aug 07, 2008 Female patient from UNITED STATES , weighting 139.0 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). Patient had the following side effects: convulsion, malaise, migraine (What is migraine?). Mysoline dosage: (250 Mg Bid Oral). During the same period patient was treated with DEPAKOTE (View Depakote Review and Depakote Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), PERCOCET (View Percocet Review and Percocet Label ), ALLEGRA (View Allegra Review and Allegra Label ).

5872997-4 | Convulsion, Decreased Activity, Dizziness, Dysphagia, Feeling Abnormal, Visual Impairment, Withdrawal Syndrome
Patient was taking Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: convulsion, decreased activity, dizziness (What is dizziness?), dysphagia, feeling abnormal, visual impairment, withdrawal syndrome on Aug 18, 2008 from UNITED STATES Additional patient health information: Female patient , 58 years of age, weighting 132.0 lb, was diagnosed with convulsion and. Mysoline dosage: 50 Mg 5 X/day Oral. During the same period patient was treated with DILANTIN /0007401/ (View Dilantin /0007401/ Review and Dilantin /0007401/ Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), NEXIUM /01479392/. (View Nexium /01479392/. Review and Nexium /01479392/. Label ), TRICOR (View Tricor Review and Tricor Label ), ZYPREXA (View Zyprexa Review and Zyprexa Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).

5872796-3 | Asthenia, Blood Glucose Increased, Convulsion, Fall, Fatigue, Weight Decreased
Adverse event was reported on Aug 18, 2008 by a Female patient taking Mysoline (View Usage) (Dosage: (250 Mg Tid Oral), (250 Mg Tid Oral)) was diagnosed with epilepsy (What is epilepsy?) and. Location: UNITED STATES , 59 years of age, weighting 248.0 lb, Patient experienced the following unwanted or unexpected effects: asthenia, blood glucose increased, convulsion, fall (What is fall?), fatigue, weight decreased. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), ACTOS (View Actos Review and Actos Label ), VYTORIN (View Vytorin Review and Vytorin Label ), LASIX (View Lasix Review and Lasix Label ).

5831441-3 | Convulsion, Dizziness
on Jul 14, 2008 Female patient from UNITED STATES , 57 years of age, weighting 128.0 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). Patient had the following side effects: convulsion, dizziness (What is dizziness?). Mysoline dosage: (250 Mg Tid Oral).

5786728-X | Balance Disorder, Feeling Abnormal, Lethargy, Nausea, Overdose, Tremor, Vertigo
on Jun 10, 2008 Female patient from UNITED STATES , 25 years of age, was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: balance disorder, feeling abnormal, lethargy, nausea (What is nausea?), overdose, tremor, vertigo. Mysoline dosage: (df).

5784228-4 | Blood Homocysteine Increased, Blood Pressure Increased, Blood Triglycerides Increased, Disorientation, Dizziness, Dysarthria, Facial Palsy, Haemorrhage Intracranial
Patient was taking Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: blood homocysteine increased, blood pressure increased, blood triglycerides increased, disorientation, dizziness (What is dizziness?), dysarthria, facial palsy, haemorrhage intracranial on May 16, 2008 from UNITED STATES Additional patient health information: Male patient , 70 years of age, was diagnosed with essential tremor, coronary artery bypass (What is coronary artery bypass?) and. Mysoline dosage: 100 Mg Bid Po, Formulation. During the same period patient was treated with PROPRANOLOL (40 Mg Bid Po, Formulation:) (View Propranolol Review and Propranolol Label ), ASPIRIN (Total Daily Dose: 81 Mg/ Total Daily Dose: 81 Mg) (View Aspirin Review and Aspirin Label ), PLENDIL (View Plendil Review and Plendil Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ), MONOPRIL (FOSONOPRIL SODIUM) (View Monopril (fosonopril Sodium) Review and Monopril (fosonopril Sodium) Label ), VASERETIC (View Vaseretic Review and Vaseretic Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

5629571-4 | Rash
Adverse event was reported on Feb 13, 2008 by a Male patient taking Mysoline (View Usage) (Dosage: 250mg 3/d Po) . Location: UNITED STATES , 40 years of age, Patient had the following side effects: rash (What is rash?).

5587984-3 | Grand Mal Convulsion
on Jan 08, 2008 Male patient from UNITED STATES , weighting 121.3 lb, was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: grand mal convulsion. Mysoline dosage: .

5483938-6 | No Adverse Reaction
on Oct 09, 2007 Female patient from UNITED STATES , weighting 170.0 lb, was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: no adverse reaction. Mysoline dosage: 50 Bid Po. Patient was hospitalized.

5424841-7 | Activities Of Daily Living Impaired, Aphonia, Asthenia, Crying, Hand Deformity, Hypoaesthesia, Hypotonia, Insomnia, Musculoskeletal Stiffness
Patient was taking Mysoline (View Usage). Patient had the following side effects: activities of daily living impaired, aphonia, asthenia, crying, hand deformity, hypoaesthesia, hypotonia, insomnia, musculoskeletal stiffness on Aug 06, 2007 from UNITED STATES Additional patient health information: Female patient , 75 years of age, weighting 175.0 lb, was diagnosed with essential tremor and. Mysoline dosage: (250 Mg Qd Oral), (250 Mg Qd Oral), (350 Mg Qd Oral). During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), TOPAMAX (View Topamax Review and Topamax Label ), HYZAAR (View Hyzaar Review and Hyzaar Label ), CRESTOR (View Crestor Review and Crestor Label ), KLONOPIN (View Klonopin Review and Klonopin Label ).

5341605-3 | Rett's Disorder
Adverse event was reported on May 29, 2007 by a Female patient taking Mysoline (View Usage) (Dosage: 250mg/ml Oral) was diagnosed with rett's disorder and. Location: UNITED STATES , 20 years of age, weighting 148.0 lb, After Mysoline was administered, patient had the following side effects: rett's disorder.

5122925-4 | Schizophrenia
on Sep 19, 2006 Male patient from UNITED STATES , 58 years of age, was diagnosed with tremor and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: schizophrenia. Mysoline dosage: 50 Mg Qday Po. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

5112884-2 | Dizziness, Gait Disturbance, Speech Disorder, Tremor
on Sep 21, 2006 Female patient from UNITED STATES , 76 years of age, weighting 217.0 lb, was diagnosed with essential tremor and was treated with Mysoline (View Usage). Patient had the following side effects: dizziness (What is dizziness?), gait disturbance, speech disorder, tremor. Mysoline dosage: 50 Mg Tid Oral.

5066324-2 | Schizophrenia
Patient was taking Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: schizophrenia on Jul 11, 2006 from UNITED STATES Additional patient health information: Male patient , 58 years of age, was diagnosed with tremor and. Mysoline dosage: 50 Mg Qday Po. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

4892452-8 | Contraindication To Medical Treatment, Grand Mal Convulsion
Adverse event was reported on Jan 25, 2006 by a Male patient taking Mysoline (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 121.3 lb, Patient experienced the following unwanted or unexpected effects: contraindication to medical treatment, grand mal convulsion.

4889801-3 | Mental Status Changes, Overdose
on Jan 05, 2006 Male patient from UNITED STATES , 69 years of age, weighting 184.0 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). Patient had the following side effects: mental status changes, overdose. Mysoline dosage: Df Once Po. During the same period patient was treated with ABILIFY (View Abilify Review and Abilify Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), M.V.I. (View M.v.i. Review and M.v.i. Label ), NEXIUM (View Nexium Review and Nexium Label ), NEFAZODONE HCL (View Nefazodone Hcl Review and Nefazodone Hcl Label ). Patient was hospitalized.

4767893-X | Mental Status Changes, Overdose
on Aug 26, 2005 Male patient from UNITED STATES , 69 years of age, weighting 184.0 lb, was diagnosed with convulsion and was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: mental status changes, overdose. Mysoline dosage: Df Once; Po. Patient was hospitalized.

4697814-X | Feeling Abnormal
Patient was taking Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: feeling abnormal on Jun 19, 2005 from Additional patient health information: Male patient , 40 years of age, weighting 180.0 lb, was diagnosed with convulsion and. Mysoline dosage: 350 Mg 1 Tab Am 2 At Hs. During the same period patient was treated with DILANTIN (100 Mg 1 Tab Am 2 At Hs) (View Dilantin Review and Dilantin Label ).

4697739-X | Tremor
Adverse event was reported on Jan 19, 2005 by a Male patient taking Mysoline (View Usage) (Dosage: 50 Mg Orally 3x Q Day) was diagnosed with tremor and. Location: , weighting 219.0 lb, Patient had the following side effects: tremor.

4696779-4 | Convulsion
on Jan 20, 2005 Female patient from , child 4 years of age, was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: convulsion. Mysoline dosage: One Po Am Three Po Pm 250. During the same period patient was treated with TEGRETOL (200 Mg Po Bid) (View Tegretol Review and Tegretol Label ). Patient was hospitalized and became disabled.

4694812-7 | Convulsion, Headache
on Jun 01, 2005 Female patient from , 69 years of age, weighting 103.4 lb, was diagnosed with epilepsy (What is epilepsy?), ex-smoker and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, headache (What is headache?). Mysoline dosage: 250 Mg Bid Po. During the same period patient was treated with COMMIT (Df Qday Po) (View Commit Review and Commit Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

4658546-7 | Condition Aggravated, Convulsion, Headache, Hypersomnia, Somnolence
Patient was taking Mysoline (View Usage). Patient had the following side effects: condition aggravated, convulsion, headache (What is headache?), hypersomnia, somnolence on Apr 21, 2005 from Additional patient health information: Male patient , 54 years of age, weighting 173.0 lb, was diagnosed with grand mal convulsion and. Mysoline dosage: 250 Mg Bid Po. During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), DILANTIN (View Dilantin Review and Dilantin Label ).

4634759-5 | Convulsion, Headache
Adverse event was reported on Mar 25, 2005 by a Female patient taking Mysoline (View Usage) (Dosage: 250 Mg Bid Po) was diagnosed with epilepsy (What is epilepsy?) and. Location: , 69 years of age, weighting 103.4 lb, After Mysoline was administered, patient had the following side effects: convulsion, headache (What is headache?). During the same period patient was treated with COMMIT (Df Qday Po) (View Commit Review and Commit Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

4626451-8 | Convulsion, Loss Of Consciousness
on Mar 14, 2005 Male patient from , 62 years of age, weighting 210.0 lb, was diagnosed with convulsion, bronchitis (What is bronchitis?), hypersensitivity, pulmonary congestion and was treated with Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, loss of consciousness. Mysoline dosage: 250 Mg Bid Po. During the same period patient was treated with THEOPHYLLINE (600 Mg Qday Po) (View Theophylline Review and Theophylline Label ), AVANDIA (View Avandia Review and Avandia Label ), SINGULAIR ^DIECKMANN^ (View Singulair ^dieckmann^ Review and Singulair ^dieckmann^ Label ), MULIVITAMIN ^FORTEX^ (View Mulivitamin ^fortex^ Review and Mulivitamin ^fortex^ Label ).

4603193-6 | Bradycardia, Convulsion, Sinus Tachycardia
on Feb 17, 2005 Female patient from , 45 years of age, was diagnosed with temporal lobe epilepsy and was treated with Mysoline (View Usage). Patient had the following side effects: bradycardia, convulsion, sinus tachycardia. Mysoline dosage: Df. During the same period patient was treated with CARBAMAZEPINE (Df) (View Carbamazepine Review and Carbamazepine Label ).

4594758-9 | Convulsion, Loss Of Consciousness
Patient was taking Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: convulsion, loss of consciousness on Feb 07, 2005 from Additional patient health information: Male patient , 62 years of age, was diagnosed with convulsion, bronchitis (What is bronchitis?), hypersensitivity, pulmonary congestion and. Mysoline dosage: 250 Mg Bid Po. During the same period patient was treated with THEOPHYLLINE (600 Mg Qday Po) (View Theophylline Review and Theophylline Label ), AVANDIA (View Avandia Review and Avandia Label ), SINGULAIR (View Singulair Review and Singulair Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

4566140-1 | Convulsion
Adverse event was reported on Jan 10, 2005 by a Female patient taking Mysoline (View Usage) (Dosage: ) . Location: , weighting 220.0 lb, Patient experienced the following unwanted or unexpected effects: convulsion.

4565841-9 | Abdominal Pain, Colitis, Diarrhoea, Faecal Occult Blood Positive, Prothrombin Time Shortened, Weight Decreased
on Jan 12, 2005 Female patient from , 43 years of age, was treated with Mysoline (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), colitis, diarrhoea, faecal occult blood positive, prothrombin time shortened, weight decreased. Mysoline dosage: 250 Mg Qday Po. During the same period patient was treated with SEGLOR LYOC (5 Mg Bid Po) (View Seglor Lyoc Review and Seglor Lyoc Label ), DEROXAT (20 Mg Qday Po) (View Deroxat Review and Deroxat Label ), URBANYL (Tab Po) (View Urbanyl Review and Urbanyl Label ). Patient was hospitalized.

4562491-5 | Condition Aggravated, Convulsion
on Jan 12, 2005 Female patient from , weighting 169.0 lb, was diagnosed with epilepsy (What is epilepsy?) and was treated with Mysoline (View Usage). After Mysoline was administered, patient had the following side effects: condition aggravated, convulsion. Mysoline dosage: [years]. During the same period patient was treated with DILANTIN (View Dilantin Review and Dilantin Label ).

4552886-8 | Condition Aggravated, Convulsion
Patient was taking Mysoline (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, convulsion on Jan 12, 2005 from Additional patient health information: Female patient , child 4 years of age, . Mysoline dosage: 200 1 P.o. Am 3 Po Pm. During the same period patient was treated with TEGRETOL (Tegretol Xr 200mg Po Bid) (View Tegretol Review and Tegretol Label ). Patient was hospitalized.