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HYPOVOLAEMIC SHOCK side effect

What is HYPOVOLAEMIC SHOCK ?
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Drugs associated with HYPOVOLAEMIC SHOCK

ABATACEPT  ACYCLOVIR  ALTACE  ARIXTRA  ASPIRIN  AVELOX  BUSULFAN  CARBOPLATIN  CEFTRIAXONE  CERTICAN  CHORIONIC  CIFLOX  CISPLATIN  COLCHICUM  COUMADIN  CUBICIN  DASATINIB  DOCETAXEL  FABRAZYME  FLUDARABINE  FOLLITROPIN  HUMIRA  HYDROXYCHLOROQUI INDOMETHACIN  ISOPTIN  JOSACINE  KALETRA  KARVEA  LANTUS  LAPATINIB  LASIX  MICARDIS  MIFEPREX  MIFEPRISTONE  PACLITAXEL  PIROXICAM  PROGRAF  RIFAMPICIN  RITONAVIR  TAXOTERE  TENORETIC  TIGECYCLINE  TIROFIBAN  TRAMADOL  ULTRAVIST  UROFOLLITROPIN  XIGRIS  ZETIA  


Carboplatin Side Effects Report #5614208-0
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on Feb 04, 2008. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PEMETREXED DI, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5614211-0
CARBOPLATIN problem was reported by a Health Professional from UNITED STATES on Feb 04, 2008. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with ALIMTA, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5598501-6
Consumer or non-health professional from NETHERLANDS reported HUMIRA problem on Jan 14, 2008. Female patient, weighting 154.3 lb, was diagnosed with rheumatoid arthritis, vitamin supplementation, hypertension, blood cholesterol and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, splenic haemorrhage, visceral leishmaniasis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, SELOCOMB, ZOCOR. Patient was hospitalized. Patient died on 02/01/2006.

Humira Side Effects Report #5570949-5
HUMIRA problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 17, 2007. Female patient, weighting 154.3 lb, was diagnosed with rheumatoid arthritis, vitamin supplementation, hypertension, blood cholesterol and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, splenic haemorrhage, visceral leishmaniasis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, SELOCOMB, ZOCOR. Patient was hospitalized. Patient died on 02/01/2006.


Karvea Side Effects Report #5503775-3
Health Professional from ITALY reported KARVEA problem on Oct 18, 2007. Female patient, 81 years of age, was diagnosed with essential hypertension, osteoarthritis and was treated with KARVEA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . KARVEA dosage: unknown. During the same period patient was treated with LASIX, TENORETIC, NORVASC, VOLTAREN. Patient was hospitalized. Patient recovered.

Busulfan Side Effects Report #5506837-X
BUSULFAN problem was reported by a Consumer or non-health professional from JAPAN on Oct 24, 2007. Male patient, 60 years of age, was diagnosed with prophylaxis against graft versus host disease, antibiotic prophylaxis, antiviral prophylaxis, antifungal prophylaxis and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, immune system disorder, pulmonary alveolar haemorrhage, thrombocytopenia, . BUSULFAN dosage: 4 MG/KG, DAY-6 TO -5. During the same period patient was treated with TACROLIMUS, FLUDARA, CIPROFLOXACIN, ACYCLOVIR, ITRACONAZOLE. Patient died on 01/01/2005.

Fludarabine Side Effects Report #5506844-7
Physician from JAPAN reported FLUDARABINE PHOSPHATE problem on Oct 24, 2007. Male patient, 60 years of age, was diagnosed with antifungal prophylaxis, antiviral prophylaxis and was treated with FLUDARABINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, immune system disorder, pulmonary alveolar haemorrhage, thrombocytopenia, . FLUDARABINE PHOSPHATE dosage: 30 MG/KG, UNK. During the same period patient was treated with BUSULFAN, TACROLIMUS, CIPROFLOXACIN, ITRACONAZOLE, ACYCLOVIR. Patient died on 01/01/2005.

Ritonavir Side Effects Report #5519982-X
RITONAVIR SOFT GELATIN CAPSULES problem was reported by a Consumer or non-health professional from BRAZIL on Nov 07, 2007. Female patient, weighting 149.7 lb, was diagnosed with hiv infection, antifungal prophylaxis and was treated with RITONAVIR SOFT GELATIN CAPSULES. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, pneumonia, septic shock, vaginal haemorrhage, . RITONAVIR SOFT GELATIN CAPSULES dosage: unknown. During the same period patient was treated with LAMIVUDINE, STAVUDINE, TENOFOVIR DISOPROXIL FUMARATE, PENTAMIDINE ISETHIONATE. Patient was hospitalized. Patient died on 08/08/2007.

Arixtra Side Effects Report #5520851-X
Physician from FRANCE reported ARIXTRA problem on Nov 09, 2007. Female patient, 67 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, peritoneal haemorrhage, shock haemorrhagic, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOVENOX. Patient was hospitalized. Patient recovered.


Fludarabine Side Effects Report #5487093-8
FLUDARABINE PHOSPHATE problem was reported by a Physician from JAPAN on Oct 02, 2007. Male patient, 60 years of age, was diagnosed with antifungal prophylaxis, antiviral prophylaxis, multiple myeloma and was treated with FLUDARABINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, immune system disorder, pulmonary alveolar haemorrhage, thrombocytopenia, . FLUDARABINE PHOSPHATE dosage: 30 MG/KG, UNK. During the same period patient was treated with BUSULFAN, TACROLIMUS, CIPROFLOXACIN, ITRACONAZOLE, ACYCLOVIR, BLOOD AND RELATED PRODUCTS. Patient died on 01/01/2005.

Tenoretic Side Effects Report #5492258-5
Health Professional from ITALY reported TENORETIC problem on Oct 18, 2007. Female patient, 82 years of age, was diagnosed with essential hypertension, osteoarthritis and was treated with TENORETIC. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . TENORETIC dosage: 100+25 MG. During the same period patient was treated with KARVEA, LASIX, NORVASC, VOLTAREN. Patient was hospitalized. Patient recovered.

Karvea Side Effects Report #5492962-9
KARVEA problem was reported by a Health Professional from ITALY on Oct 18, 2007. Female patient, 81 years of age, was diagnosed with essential hypertension, osteoarthritis and was treated with KARVEA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . KARVEA dosage: unknown. During the same period patient was treated with TENORETIC, LASIX, NORVASC, VOLTAREN. Patient was hospitalized. Patient recovered.

Karvea Side Effects Report #5501566-0
Health Professional from ITALY reported KARVEA problem on Oct 26, 2007. Female patient, 81 years of age, was diagnosed with essential hypertension, osteoarthritis and was treated with KARVEA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . KARVEA dosage: unknown. During the same period patient was treated with LASIX, TENORETIC, NORVASC, VOLTAREN. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5458618-3
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2007. Male patient, 43 years of age, was diagnosed with gastric cancer, abdominal pain, gastritis prophylaxis, nausea and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, malignant neoplasm progression, metabolic encephalopathy, renal failure acute, . CISPLATIN dosage: unknown. During the same period patient was treated with OXYCODONE, RANITIDINE, ONDANSETRON. Patient was hospitalized. Patient died on 11/23/2006.


Carboplatin Side Effects Report #5386508-3
Health Professional from UNITED STATES reported CARBOPLATIN problem on July 12, 2007. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with ALIMTA, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Ceftriaxone Side Effects Report #5388071-X
CEFTRIAXONE problem was reported by a Consumer or non-health professional from FRANCE on July 04, 2007. Male patient was diagnosed with urinary tract infection and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CEFTRIAXONE dosage: unknown. During the same period patient was treated with GENTAMICIN. Patient recovered.

Carboplatin Side Effects Report #5395205-X
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on July 23, 2007. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PEMETREXED DI, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5401378-2
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on July 25, 2007. Female patient, 67 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, peritoneal haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Carboplatin Side Effects Report #5386508-3
Health Professional from UNITED STATES reported CARBOPLATIN problem on July 12, 2007. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with ALIMTA, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.


Ceftriaxone Side Effects Report #5388071-X
CEFTRIAXONE problem was reported by a Consumer or non-health professional from FRANCE on July 04, 2007. Male patient was diagnosed with urinary tract infection and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CEFTRIAXONE dosage: unknown. During the same period patient was treated with GENTAMICIN. Patient recovered.

Carboplatin Side Effects Report #5395205-X
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on July 23, 2007. Male patient, 61 years of age, weighting 198.4 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PEMETREXED DI, FOLIC ACID, VITAMIN B, ATENOLOL, LEVOTHYROXINE, ACTOS, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5401378-2
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on July 25, 2007. Female patient, 67 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, peritoneal haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Kaletra Side Effects Report #5761274-8
Consumer or non-health professional from MEXICO reported KALETRA problem on June 04, 2008. Male patient was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . KALETRA dosage: 800/200MG DAILY, 400/100 MG TWICE DAILY. Patient died on 12/23/2006.

Humira Side Effects Report #5766226-X
HUMIRA problem was reported by a Consumer or non-health professional from NETHERLANDS on June 02, 2008. Female patient, weighting 154.3 lb, was diagnosed with rheumatoid arthritis, vitamin supplementation, hypertension, blood cholesterol and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, splenic haemorrhage, visceral leishmaniasis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, SELOCOMB, ZOCOR. Patient was hospitalized. Patient died on 02/01/2006.

Kaletra Side Effects Report #5782271-2
Consumer or non-health professional from MEXICO reported KALETRA problem on June 19, 2008. Male patient was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, . KALETRA dosage: 800/200MG DAILY, 400/100 MG TWICE DAILY. Patient died on 12/23/2006.

Avelox Side Effects Report #5786863-6
AVELOX problem was reported by a Physician from ITALY on June 20, 2008. Female patient, 39 years of age, was diagnosed with bronchiectasis, psoriasis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, urticaria, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with RAPTIVA. Patient recovered.

Cisplatin Side Effects Report #5727173-2
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Apr 30, 2008. Male patient, 43 years of age, was diagnosed with gastric cancer, abdominal pain, gastritis prophylaxis, nausea and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, malignant neoplasm progression, metabolic encephalopathy, renal failure acute, . CISPLATIN dosage: unknown. During the same period patient was treated with OXYCODONE, RANITIDINE, ONDANSETRON. Patient was hospitalized. Patient died on 11/23/2006.

Zetia Side Effects Report #5701425-4
ZETIA problem was reported by a Physician from UNITED STATES on Apr 02, 2008. Female patient, 52 years of age, was diagnosed with blood cholesterol increased and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . ZETIA dosage: unknown. During the same period patient was treated with PRAVASTATIN. Patient was hospitalized. Patient recovered.

Dasatinib Side Effects Report #5343713-X
Health Professional from UNITED STATES reported DASATINIB problem on May 29, 2007. Male patient, 43 years of age, was diagnosed with chronic myeloid leukaemia and was treated with DASATINIB. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, multi-organ failure, venous occlusion, . DASATINIB dosage: unknown. Patient died on 05/18/2007.

Humira Side Effects Report #5346215-X
HUMIRA problem was reported by a Consumer or non-health professional from NETHERLANDS on May 30, 2007. Female patient, weighting 154.3 lb, was diagnosed with rheumatoid arthritis, vitamin supplementation, hypertension, blood cholesterol and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, splenic haemorrhage, visceral leishmaniasis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, SELOCOMB, ZOCOR. Patient was hospitalized. Patient died on 02/01/2006.

Arixtra Side Effects Report #5304601-8
Physician from FRANCE reported ARIXTRA problem on Apr 12, 2007. Female patient, 61 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, operative haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Hydroxychloroqui Side Effects Report #5651543-4
HYDROXYCHLOROQUINE SULPHATE problem was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on Feb 28, 2008. Female patient, 54 years of age, was diagnosed with systemic lupus erythematosus and was treated with HYDROXYCHLOROQUINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: hypertension, hypovolaemic shock, mycotic aneurysm, oedema peripheral, salmonellosis, . HYDROXYCHLOROQUINE SULPHATE dosage: 400 MG. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Piroxicam Side Effects Report #5676382-X
Health Professional from SPAIN reported PIROXICAM problem on Mar 13, 2008. Female patient, 79 years of age, was diagnosed with myalgia and was treated with PIROXICAM. After drug was administered, patient experienced the following problems/side effects: anaemia, hypovolaemic shock, renal failure, retroperitoneal haematoma, rhabdomyolysis, . PIROXICAM dosage: unknown. During the same period patient was treated with PARACETAMOL. Patient died on 01/18/2008.

Ciflox Side Effects Report #5588232-0
CIFLOX problem was reported by a Consumer or non-health professional from FRANCE on Jan 04, 2008. Male patient, 76 years of age, was diagnosed with urinary tract infection, arrhythmia, atrial fibrillation and was treated with CIFLOX. After drug was administered, patient experienced the following problems/side effects: anaemia, hypovolaemic shock, infusion site haemorrhage, muscle haemorrhage, respiratory distress, wound haemorrhage, . CIFLOX dosage: unknown. During the same period patient was treated with PREVISCAN, CONTRAMAL, CORDARONE, ATROVENT, BRICANYL. Patient was hospitalized. Patient died on 07/23/2006.

Taxotere Side Effects Report #5595997-0
Physician from JAPAN reported TAXOTERE problem on Jan 11, 2008. Male patient, 71 years of age, weighting 112.4 lb, was diagnosed with lung adenocarcinoma recurrent, constipation, cancer pain, gastroenteritis, insomnia and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hypovolaemic shock, neutrophil count decreased, . TAXOTERE dosage: unknown. During the same period patient was treated with ALOSENN, OXYCONTIN, NAUZELIN, DEPAS, METHYCOBAL, CLONAZEPAM, LENDORMIN. Patient died on 06/24/2007.

Ciflox Side Effects Report #5597989-4
CIFLOX problem was reported by a Consumer or non-health professional from FRANCE on Jan 04, 2008. Male patient, 76 years of age, was diagnosed with urinary tract infection, arrhythmia, atrial fibrillation and was treated with CIFLOX. After drug was administered, patient experienced the following problems/side effects: anaemia, hypovolaemic shock, infusion site haemorrhage, muscle haemorrhage, respiratory distress, wound haemorrhage, . CIFLOX dosage: unknown. During the same period patient was treated with PREVISCAN, CONTRAMAL, CORDARONE, ATROVENT, BRICANYL. Patient was hospitalized. Patient died on 07/23/2006.

Taxotere Side Effects Report #5598361-3
Physician from INDIA reported TAXOTERE problem on Jan 16, 2008. Female patient, 45 years of age, weighting 242.5 lb, was diagnosed with breast cancer and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hypovolaemic shock, mucosal inflammation, renal failure acute, vomiting, . TAXOTERE dosage: unknown. Patient was hospitalized. Patient recovered.

Ciflox Side Effects Report #5537067-3
CIFLOX problem was reported by a Consumer or non-health professional from FRANCE on Nov 26, 2007. Male patient, 76 years of age, was diagnosed with urinary tract infection, arrhythmia, atrial fibrillation and was treated with CIFLOX. After drug was administered, patient experienced the following problems/side effects: anaemia, hypovolaemic shock, infusion site haemorrhage, muscle haemorrhage, respiratory distress, . CIFLOX dosage: unknown. During the same period patient was treated with PREVISCAN, CONTRAMAL, CORDARONE, ATROVENT, BRICANYL, ESIDRIX. Patient was hospitalized. Patient died on 07/23/2006.

Aspirin Side Effects Report #5574130-5
Consumer or non-health professional from UNITED KINGDOM reported ASPIRIN problem on Dec 10, 2007. Female patient, 85 years of age, was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, hypovolaemic shock, . ASPIRIN dosage: 75MG/ ORAL. During the same period patient was treated with CLOPIDOGREL, BISOPROL, FUROSEMIDE, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5574978-7
LAPATINIB problem was reported by a Physician from FRANCE on Dec 20, 2007. Female patient, 72 years of age, weighting 134.5 lb, was diagnosed with convulsion prophylaxis, breast cancer and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hypovolaemic shock, vomiting, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA, ZELITREX, RAMIPRIL, TRILEPTAL, THIOTEPA, SOLUPRED. Patient was hospitalized. Patient recovered.

Aspirin Side Effects Report #5576268-5
Health Professional from UNITED KINGDOM reported ASPIRIN problem on Dec 17, 2007. Female patient, 85 years of age, was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, hypovolaemic shock, . ASPIRIN dosage: unknown. During the same period patient was treated with CLOPIDOGREL, BISOPROLOL, AMOXICILLIN, FUROSEMIDE, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Taxotere Side Effects Report #5475473-6
TAXOTERE problem was reported by a Physician from JAPAN on Sept 28, 2007. Male patient, 71 years of age, weighting 112.4 lb, was diagnosed with lung adenocarcinoma recurrent, constipation, cancer pain, gastroenteritis, insomnia and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hypovolaemic shock, lung neoplasm malignant, . TAXOTERE dosage: unknown. During the same period patient was treated with ALOSENN, OXYCONTIN, NAUZELIN, DEPAS, METHYCOBAL, RIVOTRIL, LENDORMIN. Patient died on 06/24/2007.

Abatacept Side Effects Report #5484068-X
Health Professional from MEXICO reported ABATACEPT problem on Oct 09, 2007. Male patient, 70 years of age, weighting 108.0 lb, was treated with ABATACEPT. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, hypovolaemic shock, pneumonia, . ABATACEPT dosage: unknown. During the same period patient was treated with METHOTREXATE, CIPROXIN, OMEPRAZOLE. Patient was hospitalized. Patient died on 10/02/2007.

Abatacept Side Effects Report #5490895-5
ABATACEPT problem was reported by a Health Professional from MEXICO on Oct 09, 2007. Male patient, 70 years of age, weighting 108.0 lb, was treated with ABATACEPT. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, hypovolaemic shock, pneumonia, . ABATACEPT dosage: unknown. During the same period patient was treated with METHOTREXATE, DICLOFENAC, CIPROXIN, OMEPRAZOLE. Patient was hospitalized. Patient died on 10/02/2007.

Lasix Side Effects Report #5499194-9
Consumer or non-health professional from reported LASIX problem on Oct 18, 2007. Female patient, 81 years of age, was diagnosed with essential hypertension and was treated with LASIX. After drug was administered, patient experienced the following problems/side effects: hypovolaemic shock, renal failure acute, . LASIX dosage: unknown. During the same period patient was treated with TENORETIC, KARVEA, VOLTAREN, NORVASC. Patient recovered.

Certican Side Effects Report #5501024-3
CERTICAN problem was reported by a Physician from MALAYSIA on Oct 25, 2007. Male patient, 33 years of age, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: explorative laparotomy, hypovolaemic shock, intra-abdominal haemorrhage, multi-organ failure, sepsis, . CERTICAN dosage: unknown. During the same period patient was treated with PREDNISOLONE, NEORAL, MYFORTIC. Patient was hospitalized. Patient died on 07/09/2007.

Colchicum Side Effects Report #5420605-9
Physician from GERMANY reported COLCHICUM problem on Aug 10, 2007. Male patient, 57 years of age, was diagnosed with ill-defined disorder, hypertension and was treated with COLCHICUM. After drug was administered, patient experienced the following problems/side effects: hepatic failure, hypovolaemic shock, ileus paralytic, multi-organ failure, pancreatitis necrotising, pulmonary embolism, renal failure acute, respiratory distress, sepsis, . COLCHICUM dosage: unknown. During the same period patient was treated with COVERSUM, RANITIC. Patient died on 11/12/2003.

Tigecycline Side Effects Report #5726358-9
TIGECYCLINE problem was reported by a Physician from UNITED STATES on Apr 23, 2008. Male patient, 57 years of age, was diagnosed with osteomyelitis, mycobacterium chelonei infection and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, hypovolaemic shock, multi-organ failure, pancreatitis haemorrhagic, pancreatitis necrotising, renal failure acute, . TIGECYCLINE dosage: unknown. During the same period patient was treated with CRESTOR, LORTAB, SINGULAIR, HALCION, BIAXIN, AMIKACIN. Patient died on 07/04/2007.

Micardis Side Effects Report #5745695-5
Consumer or non-health professional from reported MICARDIS problem on May 19, 2008. Male patient, weighting 143.3 lb, was diagnosed with hypertension, insomnia, rhinitis allergic, osteoarthritis, back pain, benign prostatic hyperplasia and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: duodenal ulcer haemorrhage, hypovolaemic shock, . MICARDIS dosage: unknown. During the same period patient was treated with IMOVANE, RIVOTRIL, ADALAT, VOREN, FUBIFEN, HARNALIDGE. Patient was hospitalized. Patient died on 04/06/2008.

Micardis Side Effects Report #5748171-9
MICARDIS problem was reported by a Consumer or non-health professional from on May 21, 2008. Male patient, weighting 143.3 lb, was diagnosed with hypertension, benign prostatic hyperplasia and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: duodenal ulcer haemorrhage, hypovolaemic shock, . MICARDIS dosage: unknown. During the same period patient was treated with HARNALIDGE. Patient was hospitalized. Patient died on 04/06/2008.

Docetaxel Side Effects Report #5690890-7
Health Professional from CANADA reported DOCETAXEL problem on Mar 25, 2008. Male patient, 69 years of age, weighting 132.0 lb, was diagnosed with prostate cancer and was treated with DOCETAXEL. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hypovolaemic shock, vomiting, . DOCETAXEL dosage: unknown. During the same period patient was treated with MONOCLONAL ANTIBODIES, DILAUDID, FLOVENT, SPIRIVA, VENTOLIN, MONTELUKAST, FOSAMAX, CELEBREX. Patient died on 03/10/2008.

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