When Bonnie was concerned about staying on Paxil she was told not to be concerned as it was classified as Category B. Tragically, her son died from heart birth defects; 5 years later she found that Paxil is now Category D.
(In December 2005, the FDA asked Glaxo Smith Kline, the manufacturer of Paxil effects, to change the pregnancy category to D, a stronger warning. Category D means that studies in pregnant women have demonstrated a risk to the fetus.)
"I initial began taking Paxil effects when I was in high school," says Bonnie (not her actual name pending a lawsuit). Then I quit taking it when I got pregnant with my oldest kid - I've 4 children. But by the time I was pregnant with Keagan, my life had turn out to be challenging and I was extremely depressed; my husband's job meant that we had to move far away from family members and buddies and I began taking Paxil once more. I known as my Mum (she is really a nurse) and asked her if there was any danger in taking this drug. She looked it up within the drug book and it was a category B so there had been no warnings and no side effects -- this would have been late in 2001.
My husband lost his job again and we moved even farther away, so I stayed on Paxil effects. I gave birth to Keagan and when he was only six hours old the doctor told me that he had to be transported to Children's Hospital because his oxygen saturation was low and they had detected a heart murmur.
As soon as he was transferred, Keagan underwent his initial heart surgery. He was diagnosed with vital aortic stenosis - his aortic valve wasn't functioning correctly. They also diagnosed him with hypoplastic left heart syndrome (HLHS) -- among the rarer heart defects which indicates that the left ventricle is under-functioning or it might be non-existent. He also had endocardial fibroelastosis (EFE).
It was heartbreaking - every little thing I went by means of to remain pregnant with him after which to become told that he had serious heart defects...We had loved ones fly in from Canada, from Oregon and Washington. My sister took my youngsters back to Washington with her. I slept inside the hospital virtually each night as well as a lot of my loved ones stayed across the street,in a spot like a Ronald Macdonald Charity residence.
At three weeks old, Keagan had a ballooning of his aortic valve; he had one scheduled open heart surgery and another emergency surgery the following day. When I got to the hospital the morning of Feb 7th it had been written in his chart that family was to spend time with him and hold him as much as possible. Up to that point I hadn't been allowed to hold him.
I called my husband to come back to the hospital immediately and then it took two nurses and the respiratory therapist to move Keagan from his little bed into my arms. Between me and my family, we held him all day. Then he started having problems with blood and oxygen levels so the doctors asked if we wanted to have a 'Do Not Resuscitate' (DNR) order.
We opted for the DNR to become put in spot and referred to as members of our church; they had been so supportive. My minister, his wife along with other members from the congregation came. Items weren't enhancing. Keagan's white blood cell count went actually high and he was bleeding in 1 of his lungs. The medical doctor met with me and my husband and our minister and asked if we wanted to let him go or pursue remedy.
At that point we decided to let him go. At 10 pm, with Keagan in my arms, our minister sat in the room and prayed for about 10 minutes, then my husband and I were left alone with our son. The nurse stopped everything except for pain medication and the doctor disconnected the respirator. At 11pm his heart stopped beating.
We had a tiny service for our son and my church was great - they paid for the service and Keagan's cremation. We granted the hospital permission to autopsy his heart and lung and my husband and I consented to genetic testing. At this time I had no thought there was a connection to Paxil. Right after his autopsy outcomes came back, we had been told it was a factor that just occurred; there was no explanation.
Last week I saw a commercial on tv from a law firm, saying there was a feasible link in between Paxil effects and heart birth defects. I known as my Mum immediately and she looked it up once more in her drug book - this time it was a category danger D. Later that evening my sister looked up Paxil effects on the Internet and she stated there was a great deal of info concerning the link in between Paxil and coronary heart defects. She discovered your web site for me, and also the following day a lawyer contacted me.
I nearly did not go via with this lawsuit simply because I had come to terms with Keagan's death and now it's all fresh once more. But I do not want other parents to need to go via what I went via.
(In December 2005, the FDA asked Glaxo Smith Kline, the manufacturer of Paxil effects, to change the pregnancy category to D, a stronger warning. Category D means that studies in pregnant women have demonstrated a risk to the fetus.)
"I initial began taking Paxil effects when I was in high school," says Bonnie (not her actual name pending a lawsuit). Then I quit taking it when I got pregnant with my oldest kid - I've 4 children. But by the time I was pregnant with Keagan, my life had turn out to be challenging and I was extremely depressed; my husband's job meant that we had to move far away from family members and buddies and I began taking Paxil once more. I known as my Mum (she is really a nurse) and asked her if there was any danger in taking this drug. She looked it up within the drug book and it was a category B so there had been no warnings and no side effects -- this would have been late in 2001.
My husband lost his job again and we moved even farther away, so I stayed on Paxil effects. I gave birth to Keagan and when he was only six hours old the doctor told me that he had to be transported to Children's Hospital because his oxygen saturation was low and they had detected a heart murmur.
As soon as he was transferred, Keagan underwent his initial heart surgery. He was diagnosed with vital aortic stenosis - his aortic valve wasn't functioning correctly. They also diagnosed him with hypoplastic left heart syndrome (HLHS) -- among the rarer heart defects which indicates that the left ventricle is under-functioning or it might be non-existent. He also had endocardial fibroelastosis (EFE).
It was heartbreaking - every little thing I went by means of to remain pregnant with him after which to become told that he had serious heart defects...We had loved ones fly in from Canada, from Oregon and Washington. My sister took my youngsters back to Washington with her. I slept inside the hospital virtually each night as well as a lot of my loved ones stayed across the street,in a spot like a Ronald Macdonald Charity residence.
At three weeks old, Keagan had a ballooning of his aortic valve; he had one scheduled open heart surgery and another emergency surgery the following day. When I got to the hospital the morning of Feb 7th it had been written in his chart that family was to spend time with him and hold him as much as possible. Up to that point I hadn't been allowed to hold him.
I called my husband to come back to the hospital immediately and then it took two nurses and the respiratory therapist to move Keagan from his little bed into my arms. Between me and my family, we held him all day. Then he started having problems with blood and oxygen levels so the doctors asked if we wanted to have a 'Do Not Resuscitate' (DNR) order.
We opted for the DNR to become put in spot and referred to as members of our church; they had been so supportive. My minister, his wife along with other members from the congregation came. Items weren't enhancing. Keagan's white blood cell count went actually high and he was bleeding in 1 of his lungs. The medical doctor met with me and my husband and our minister and asked if we wanted to let him go or pursue remedy.
At that point we decided to let him go. At 10 pm, with Keagan in my arms, our minister sat in the room and prayed for about 10 minutes, then my husband and I were left alone with our son. The nurse stopped everything except for pain medication and the doctor disconnected the respirator. At 11pm his heart stopped beating.
We had a tiny service for our son and my church was great - they paid for the service and Keagan's cremation. We granted the hospital permission to autopsy his heart and lung and my husband and I consented to genetic testing. At this time I had no thought there was a connection to Paxil. Right after his autopsy outcomes came back, we had been told it was a factor that just occurred; there was no explanation.
Last week I saw a commercial on tv from a law firm, saying there was a feasible link in between Paxil effects and heart birth defects. I known as my Mum immediately and she looked it up once more in her drug book - this time it was a category danger D. Later that evening my sister looked up Paxil effects on the Internet and she stated there was a great deal of info concerning the link in between Paxil and coronary heart defects. She discovered your web site for me, and also the following day a lawyer contacted me.
I nearly did not go via with this lawsuit simply because I had come to terms with Keagan's death and now it's all fresh once more. But I do not want other parents to need to go via what I went via.
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