When Bonnie was concerned about staying on Paxil she was told not to worry 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 implies that studies in pregnant women have demonstrated a danger towards the fetus.)
"I initial started taking Paxil effects when I was in high school," says Bonnie (not her genuine name pending a lawsuit). Then I quit taking it when I got pregnant with my oldest kid - I've 4 kids. 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 and friends and I started taking Paxil once again. I called my Mum (she is really a nurse) and asked her if there was any danger in taking this drug. She looked it up in 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 once 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 physician told me that he had to become 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 critical 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 - everything I went by means of to remain pregnant with him after which to become told that he had serious heart defects...We had family members fly in from Canada, from Oregon and Washington. My sister took my children back to Washington with her. I slept inside the hospital virtually every night and a lot of my family stayed across the street,in a location like a Ronald Macdonald Charity home.
At 3 weeks old, Keagan had a ballooning of his aortic valve; he had 1 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 loved ones was to devote time with him and hold him as much as feasible. As much as that point I hadn't been allowed to hold him. I called my husband to come back to the hospital immediately after which it took two nurses and also the respiratory therapist to move Keagan from his small bed into my arms. Between me and my family members, 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 location 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. Issues weren't enhancing. Keagan's white blood cell count went really high and he was bleeding in one of his lungs. The physician met with me and my husband and our minister and asked if we wanted to let him go or pursue therapy.
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 had been left alone with our son. The nurse stopped every thing except for discomfort medication as well as the physician disconnected the respirator. At 11pm his heart stopped beating.
We had a small service for our son and my church was fantastic - 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. Following his autopsy outcomes came back, we were told it was a factor that just happened; there was no explanation.
Last week I saw a commercial on television 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 again 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 said there was a great deal of information concerning the link in between Paxil and coronary heart defects. She found your site for me, as well as the following day a lawyer contacted me. I virtually didn't go through with this lawsuit simply because I had come to terms with Keagan's death and now it's all fresh once again. But I don't want other parents to have to go through what I went by means of.
(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 implies that studies in pregnant women have demonstrated a danger towards the fetus.)
"I initial started taking Paxil effects when I was in high school," says Bonnie (not her genuine name pending a lawsuit). Then I quit taking it when I got pregnant with my oldest kid - I've 4 kids. 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 and friends and I started taking Paxil once again. I called my Mum (she is really a nurse) and asked her if there was any danger in taking this drug. She looked it up in 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 once 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 physician told me that he had to become 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 critical 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 - everything I went by means of to remain pregnant with him after which to become told that he had serious heart defects...We had family members fly in from Canada, from Oregon and Washington. My sister took my children back to Washington with her. I slept inside the hospital virtually every night and a lot of my family stayed across the street,in a location like a Ronald Macdonald Charity home.
At 3 weeks old, Keagan had a ballooning of his aortic valve; he had 1 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 loved ones was to devote time with him and hold him as much as feasible. As much as that point I hadn't been allowed to hold him. I called my husband to come back to the hospital immediately after which it took two nurses and also the respiratory therapist to move Keagan from his small bed into my arms. Between me and my family members, 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 location 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. Issues weren't enhancing. Keagan's white blood cell count went really high and he was bleeding in one of his lungs. The physician met with me and my husband and our minister and asked if we wanted to let him go or pursue therapy.
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 had been left alone with our son. The nurse stopped every thing except for discomfort medication as well as the physician disconnected the respirator. At 11pm his heart stopped beating.
We had a small service for our son and my church was fantastic - 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. Following his autopsy outcomes came back, we were told it was a factor that just happened; there was no explanation.
Last week I saw a commercial on television 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 again 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 said there was a great deal of information concerning the link in between Paxil and coronary heart defects. She found your site for me, as well as the following day a lawyer contacted me. I virtually didn't go through with this lawsuit simply because I had come to terms with Keagan's death and now it's all fresh once again. But I don't want other parents to have to go through what I went by means of.
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