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CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY side effect

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Lovenox Side Effects Report #5670572-8
Consumer or non-health professional from UNITED STATES reported LOVENOX problem on Mar 11, 2008. Female patient was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, multiple congenital abnormalities, . LOVENOX dosage: unknown. Patient recovered.

Claravis Side Effects Report #5538363-6
CLARAVIS problem was reported by a Physician from UNITED STATES on Nov 20, 2007. Male patient was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, congenital choroidal anomaly, congenital hydrocephalus, foetal cardiac disorder, head deformity, low set ears, . CLARAVIS dosage: unknown. Patient died on 10/05/2007.

Lamictal Side Effects Report #5483796-X
Consumer or non-health professional from FRANCE reported LAMICTAL problem on Oct 01, 2007. Male patient was diagnosed with epilepsy and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, talipes, . LAMICTAL dosage: 100MG TWICE PER DAY. During the same period patient was treated with DEPAKENE, GARDAN. Patient was hospitalized. Patient recovered.

Claravis Side Effects Report #5450722-9
CLARAVIS problem was reported by a Physician from UNITED STATES on Aug 27, 2007. Female patient was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, congenital choroidal anomaly, heart disease congenital, . CLARAVIS dosage: 40 MG, QD, TRANSPLACENTAL. Patient recovered.


Claravis Side Effects Report #5450723-0
Physician from UNITED STATES reported CLARAVIS problem on Sept 05, 2007. Female patient, 15 years of age, was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, heart disease congenital, neural tube defect, treatment noncompliance, ultrasound antenatal screen abnormal, unintended pregnancy, . CLARAVIS dosage: 40 MG, QD, ORAL. Patient recovered.

Valacyclovir Side Effects Report #5468197-2
VALACYCLOVIR problem was reported by a Consumer or non-health professional from FRANCE on Sept 10, 2007. Female patient was diagnosed with cytomegalovirus infection and was treated with VALACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, foetal disorder, premature baby, splenomegaly, . VALACYCLOVIR dosage: unknown. Patient recovered.

Irbesartan Side Effects Report #5409408-9
Health Professional from reported IRBESARTAN problem on Aug 07, 2007. Female patient, 24 years of age, was treated with IRBESARTAN. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, pregnancy, renal aplasia, . IRBESARTAN dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE, CALCIUM SUPPLEMENT, IRON SUPPLEMENT, EPOGEN, LEVOTHYROXINE, INSULIN. Patient recovered.

Inflammide Side Effects Report #5385109-0
INFLAMMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, weighting 7.05 lb, was diagnosed with asthma and was treated with INFLAMMIDE. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, developmental delay, hypotonia, . INFLAMMIDE dosage: unknown. Patient recovered.

Inflammide Side Effects Report #5385109-0
Consumer or non-health professional from UNITED STATES reported INFLAMMIDE problem on July 06, 2007. Female patient, weighting 7.05 lb, was diagnosed with asthma and was treated with INFLAMMIDE. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, developmental delay, hypotonia, . INFLAMMIDE dosage: unknown. Patient recovered.


Valium Side Effects Report #5749876-6
VALIUM problem was reported by a Physician from FRANCE on May 15, 2008. Female patient, 34 years of age, was diagnosed with epilepsy and was treated with VALIUM. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, . VALIUM dosage: unknown. During the same period patient was treated with ZYPREXA, ALEPSAL, URBANYL, LAMICTAL. Patient recovered.

Accutane Side Effects Report #5690567-8
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Dec 06, 1983. Male patient, weighting 4.63 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, dysmorphism, ear malformation, hydrocephalus, multiple congenital abnormalities, neonatal respiratory distress syndrome, pneumonia, polyhydramnios, . ACCUTANE dosage: unknown. During the same period patient was treated with ERYTHROMYCIN. Patient died on 12/01/1983.

Irbesartan Side Effects Report #5374562-4
IRBESARTAN problem was reported by a Health Professional from on June 22, 2007. Female patient, 24 years of age, was treated with IRBESARTAN. After drug was administered, patient experienced the following problems/side effects: congenital central nervous system anomaly, pregnancy, renal aplasia, . IRBESARTAN dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE, CALCIUM SUPPLEMENT, IRON SUPPLEMENT, EPOGEN, LEVOTHYROXINE, INSULIN. Patient recovered.

Strattera Side Effects Report #5649883-8
Physician from UNITED STATES reported STRATTERA problem on Feb 20, 2008. Male patient, weighting 74.99 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: adenotonsillectomy, congenital central nervous system anomaly, convulsion, electroencephalogram abnormal, hallucination, auditory, hallucination, visual, . STRATTERA dosage: 35 MG, EACH EVENING. During the same period patient was treated with CONCERTA. Patient recovered.

Keppra Side Effects Report #5623878-2
KEPPRA problem was reported by a Physician from FRANCE on Jan 23, 2008. Female patient was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: cerebral ventricle dilatation, congenital central nervous system anomaly, . KEPPRA dosage: 1500 MG 1/D TRP. Patient recovered.


Escitalopram Side Effects Report #5648540-1
Health Professional from PORTUGAL reported ESCITALOPRAM problem on Feb 14, 2008. Female patient was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: abortion induced, congenital central nervous system anomaly, . ESCITALOPRAM dosage: 10 MG QD TRANSPLACENTAL. Patient recovered.

Abilify Side Effects Report #5471118-X
ABILIFY problem was reported by a Physician from FRANCE on Sept 24, 2007. Female patient, 42 years of age, weighting 154.3 lb, was diagnosed with schizophrenia, hypothyroidism and was treated with ABILIFY. After drug was administered, patient experienced the following problems/side effects: abortion induced, congenital central nervous system anomaly, pregnancy, . ABILIFY dosage: unknown. During the same period patient was treated with XANAX, LEVOTHYROX. Patient recovered.

Irbesartan Side Effects Report #5411009-3
Health Professional from SPAIN reported IRBESARTAN problem on Aug 07, 2007. Female patient, 24 years of age, weighting 134.5 lb, was diagnosed with hypertension and was treated with IRBESARTAN. After drug was administered, patient experienced the following problems/side effects: abortion induced, congenital central nervous system anomaly, pregnancy, renal aplasia, . IRBESARTAN dosage: unknown. During the same period patient was treated with INSULIN GLARGINE, HYDROCHLOROTHIAZIDE, LEVOTHYROXINE. Patient recovered.

Viraferonpeg Side Effects Report #5789280-8
VIRAFERONPEG problem was reported by a Consumer or non-health professional from FRANCE on June 19, 2008. Male patient, weighting 5.62 lb, was diagnosed with hepatitis c, epilepsy and was treated with VIRAFERONPEG. After drug was administered, patient experienced the following problems/side effects: congenital anomaly, congenital central nervous system anomaly, craniosynostosis, dysmorphism, fontanelle depressed, hypotelorism of orbit, nuclear magnetic resonance imaging brain abnormal, . VIRAFERONPEG dosage: unknown. During the same period patient was treated with COPEGUS, DEPAKENE, PAROXETINE, CYSTINE B, LAMICTAL, LEVOTHYROX, DOLIPRANE, CYSTINE B. Patient recovered.

Lamictal Side Effects Report #5727669-3
Consumer or non-health professional from FRANCE reported LAMICTAL problem on Apr 22, 2008. Male patient was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: cerebral ventricle dilatation, congenital central nervous system anomaly, . LAMICTAL dosage: 100MG PER DAY. During the same period patient was treated with URBANYL, ALEPSAL, VALIUM, ZYPREXA. Patient died on 04/08/2008.


Valproate Side Effects Report #5729191-7
VALPROATE problem was reported by a Physician from FRANCE on May 06, 2008. Female patient, weighting 4.03 lb, was diagnosed with convulsion prophylaxis and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: bone disorder, congenital central nervous system anomaly, congenital eyelid malformation, congenital hydrocephalus, developmental delay, dysmorphism, educational problem, foetal anticonvulsant syndrome, . VALPROATE dosage: unknown. Patient recovered.

Zoloft Side Effects Report #5254889-7
Physician from UNITED STATES reported ZOLOFT problem on Mar 02, 2007. Female patient, weighting 7.50 lb, was diagnosed with anxiety, depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: cerebral cyst, congenital central nervous system anomaly, feeding disorder neonatal, polydactyly, tremor, . ZOLOFT dosage: unknown. Patient recovered.

Keppra Side Effects Report #5625923-7
KEPPRA problem was reported by a Physician from FRANCE on Jan 24, 2008. Female patient was diagnosed with epilepsy and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: brain malformation, cerebral ventricle dilatation, congenital central nervous system anomaly, foetal malformation, . KEPPRA dosage: 1500 MG 1/D TRP. Patient recovered.

Lamictal Side Effects Report #5529368-X
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Nov 20, 2007. Female patient, weighting 6.83 lb, was diagnosed with bipolar disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: brain malformation, cerebral ventricle dilatation, congenital central nervous system anomaly, developmental delay, hydrocephalus, . LAMICTAL dosage: unknown. During the same period patient was treated with KLONOPIN, PROZAC, XANAX, ATIVAN. Patient recovered.

Depas Side Effects Report #5476574-9
DEPAS problem was reported by a Health Professional from JAPAN on Sept 27, 2007. Male patient, weighting 8.40 lb, was treated with DEPAS. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood urine present, congenital central nervous system anomaly, decreased activity, exercise lack of, feeding disorder, hypercreatininaemia, . DEPAS dosage: unknown. During the same period patient was treated with ALPRAZOLAM, LUDIOMIL. Patient was hospitalized. Patient recovered.

Claravis Side Effects Report #5495451-0
Physician from UNITED STATES reported CLARAVIS problem on Oct 08, 2007. Male patient was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: apgar score low, congenital anomaly, congenital central nervous system anomaly, congenital choroidal anomaly, head deformity, heart disease congenital, low set ears, . CLARAVIS dosage: 40 MG, QD, TRANSPLACENTAL. Patient died on 10/05/2007.

Depas Side Effects Report #5467785-7
DEPAS problem was reported by a Consumer or non-health professional from JAPAN on Sept 19, 2007. Male patient, weighting 8.38 lb, was treated with DEPAS. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood urine present, congenital central nervous system anomaly, decreased activity, exercise lack of, feeding disorder, hypercreatininaemia, . DEPAS dosage: unknown. During the same period patient was treated with ALPRAZOLAM, LUDIOMIL. Patient was hospitalized. Patient recovered.

Valacyclovir Side Effects Report #5468199-6
Consumer or non-health professional from FRANCE reported VALACYCLOVIR problem on Sept 10, 2007. Female patient was diagnosed with cytomegalovirus infection and was treated with VALACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: abortion induced, brain damage, congenital central nervous system anomaly, congenital cerebral cyst, foetal disorder, . VALACYCLOVIR dosage: unknown. Patient recovered.

Accutane Side Effects Report #5690565-4
ACCUTANE problem was reported by a Physician from UNITED STATES on Sept 26, 1983. Female patient, weighting 3.31 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: bronchopleural fistula, congenital cardiovascular anomaly, congenital central nervous system anomaly, dysmorphism, ear malformation, premature baby, . ACCUTANE dosage: unknown. Patient died on 02/16/1984.

Alteis Side Effects Report #5706335-4
Consumer or non-health professional from FRANCE reported ALTEIS problem on Mar 27, 2008. Male patient, weighting 1.79 lb, was diagnosed with hypertension and was treated with ALTEIS. After drug was administered, patient experienced the following problems/side effects: abortion induced, congenital bladder anomaly, congenital central nervous system anomaly, foetal growth retardation, multiple congenital abnormalities, oligohydramnios, potter's syndrome, . ALTEIS dosage: unknown. During the same period patient was treated with LODOZ. Patient died on 01/01/2008.

Lodoz Side Effects Report #5712116-8
LODOZ problem was reported by a Consumer or non-health professional from FRANCE on Mar 28, 2008. Male patient was treated with LODOZ. After drug was administered, patient experienced the following problems/side effects: cerebral hypoperfusion, congenital bladder anomaly, congenital central nervous system anomaly, foetal disorder, foetal growth retardation, multiple congenital abnormalities, potter's syndrome, . LODOZ dosage: unknown. During the same period patient was treated with OLMESARTAN MEDOXOMIL. Patient was hospitalized. Patient died.

Depakene Side Effects Report #5320931-8
Physician from FRANCE reported DEPAKENE problem on Apr 30, 2007. Female patient, 32 years of age, was diagnosed with epilepsy, vitamin supplementation, cardiovascular event prophylaxis and was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: caesarean section, congenital anomaly, congenital central nervous system anomaly, convulsion, hospitalisation, intrauterine infection, neonatal respiratory distress syndrome, partial seizures, . DEPAKENE dosage: unknown. During the same period patient was treated with FOLIC ACID, VINPOCETINE. Patient was hospitalized. Patient recovered.

Ludiomil Side Effects Report #5339729-X
LUDIOMIL problem was reported by a Consumer or non-health professional from JAPAN on May 23, 2007. Male patient, weighting 8.40 lb, was treated with LUDIOMIL. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood urine present, congenital central nervous system anomaly, decreased activity, exercise lack of, feeding disorder, hypercreatininaemia, hyporeflexia, . LUDIOMIL dosage: unknown. During the same period patient was treated with ETIZOLAM, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Depas Side Effects Report #5339738-0
Consumer or non-health professional from JAPAN reported DEPAS problem on May 23, 2007. Male patient, weighting 8.38 lb, was treated with DEPAS. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood urine present, congenital central nervous system anomaly, decreased activity, exercise lack of, feeding disorder, hypercreatininaemia, . DEPAS dosage: unknown. During the same period patient was treated with SOLANAX, LUDIOMIL. Patient was hospitalized. Patient recovered.

Ludiomil Side Effects Report #5293074-X
LUDIOMIL problem was reported by a Consumer or non-health professional from JAPAN on Apr 02, 2007. Male patient, weighting 8.40 lb, was treated with LUDIOMIL. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood urine present, congenital central nervous system anomaly, decreased activity, exercise lack of, feeding disorder, hypercreatininaemia, hyporeflexia, . LUDIOMIL dosage: unknown. During the same period patient was treated with ETIZOLAM, ALPRAZOLAM. Patient was hospitalized. Patient recovered.