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LIMB REDUCTION DEFECT side effect

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Micronor Side Effects Report #5601197-8
Health Professional from UNITED KINGDOM reported MICRONOR problem on Jan 16, 2008. Female patient, weighting 7.85 lb, was treated with MICRONOR. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, . MICRONOR dosage: unknown. Patient recovered.

Bevacizumab Side Effects Report #5508373-3
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 29, 2007. Male patient, weighting 6.70 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: limb reduction defect, . BEVACIZUMAB dosage: unknown. During the same period patient was treated with ERLOTINIB. Patient recovered.

Pentasa Side Effects Report #5382862-7
Physician from UNITED STATES reported PENTASA problem on July 03, 2007. Female patient, 29 years of age, weighting 125.0 lb, was diagnosed with crohn's disease and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, pregnancy, . PENTASA dosage: unknown. Patient recovered.

Pentasa Side Effects Report #5391813-0
PENTASA problem was reported by a Physician from UNITED STATES on July 02, 2007. Female patient was diagnosed with crohn's disease and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: congenital hand malformation, limb reduction defect, . PENTASA dosage: unknown. Patient recovered.


Pentasa Side Effects Report #5382862-7
Physician from UNITED STATES reported PENTASA problem on July 03, 2007. Female patient, 29 years of age, weighting 125.0 lb, was diagnosed with crohn's disease and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, pregnancy, . PENTASA dosage: unknown. Patient recovered.

Pentasa Side Effects Report #5391813-0
PENTASA problem was reported by a Physician from UNITED STATES on July 02, 2007. Female patient was diagnosed with crohn's disease and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: congenital hand malformation, limb reduction defect, . PENTASA dosage: unknown. Patient recovered.

Keppra Side Effects Report #5370524-1
Physician from GERMANY reported KEPPRA problem on June 06, 2007. Male patient, weighting 7.21 lb, was diagnosed with grand mal convulsion and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, . KEPPRA dosage: 2500 MG/ /D TRP. During the same period patient was treated with LAMOTRIGINE. Patient recovered.

Keppra Side Effects Report #5339335-7
KEPPRA problem was reported by a Consumer or non-health professional from GERMANY on May 16, 2007. Female patient was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, . KEPPRA dosage: unknown. Patient recovered.

Cymbalta Side Effects Report #5273367-2
Physician from UNITED KINGDOM reported CYMBALTA problem on Mar 12, 2007. Female patient was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: limb reduction defect, . CYMBALTA dosage: unknown. During the same period patient was treated with MIRTAZAPINE. Patient recovered.


Lamotrigine Side Effects Report #5537366-5
LAMOTRIGINE problem was reported by a Health Professional from UNITED STATES on Nov 29, 2007. Female patient was diagnosed with bipolar disorder and was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: limb malformation, limb reduction defect, . LAMOTRIGINE dosage: 200MG PER DAY. During the same period patient was treated with LEXAPRO, VITAMIN CAP. Patient recovered.

Lamotrigine Side Effects Report #5547205-4
Health Professional from UNITED STATES reported LAMOTRIGINE problem on Dec 05, 2007. Female patient was diagnosed with bipolar disorder and was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: limb malformation, limb reduction defect, . LAMOTRIGINE dosage: 200MG PER DAY. During the same period patient was treated with LEXAPRO, VITAMIN CAP. Patient recovered.

Erlotinib Side Effects Report #5525738-4
ERLOTINIB problem was reported by a Physician from UNITED STATES on Nov 07, 2007. Male patient, weighting 6.61 lb, was diagnosed with non-small cell lung cancer metastatic and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: congenital hand malformation, limb reduction defect, . ERLOTINIB dosage: unknown. During the same period patient was treated with BEVACIZUMAB. Patient recovered.

Thalidomide Side Effects Report #5473155-8
Physician from BRAZIL reported THALIDOMIDE problem on Sept 18, 2007. Female patient was diagnosed with leprosy and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: heart disease congenital, limb reduction defect, . THALIDOMIDE dosage: unknown. Patient died.

Sertraline Side Effects Report #5413302-7
SERTRALINE problem was reported by a Health Professional from UNITED KINGDOM on July 12, 2007. Female patient was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: congenital anomaly, limb reduction defect, . SERTRALINE dosage: unknown. Patient recovered.


Xolair Side Effects Report #5326291-0
Physician from SWITZERLAND reported XOLAIR problem on May 07, 2007. Male patient, 77 years of age, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: allergic granulomatous angiitis, cardiomyopathy, limb reduction defect, nervousness, pulmonary embolism, vasculitis cerebral, . XOLAIR dosage: 375 MG, 2/WEEK. Patient was hospitalized. Patient recovered.