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FAILURE TO THRIVE side effect

What is FAILURE TO THRIVE ?
Help Community - Describe Your Side Effect   Search FDA Side Effects   Ask Health Expert   FAILURE TO THRIVE and Recently Reported Side Effects   FAILURE TO THRIVE and 15 most Active Side Effect polls   FAILURE TO THRIVE and featured health surveys   Substances toxic to Health   Recent Hospital reviews   Comments about Side Effects   Hospital Quality reviews   Homecare Quality reviews
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Drugs associated with FAILURE TO THRIVE

AMEVIVE  ARAVA  AREDIA  ARIXTRA  AUGMENTIN  AVASTIN  AVONEX  BEVACIZUMAB  BEXTRA  BISOPROLOL  BLOPRESS  BONIVA  CAP  CARBOPLATIN  CETUXIMAB  CISPLATIN  CYCLOPHOSPHAMIDE CYCLOSPORINE  DEROXAT  DESFLURANE  DIANEAL  DIDANOSINE  DOCETAXEL  DOXORUBICIN  EFFEXOR  EMEND  ERLOTINIB  FAMOTIDINE  FENTANYL  FORTEO  HUMATROPE  INFLIXIMAB  KALETRA  KEPPRA  LAMOTRIGINE  LAPATINIB  LIORESAL  LOVENOX  MYOZYME  NEXAVAR  OXALIPLATIN  OXYCONTIN  PACLITAXEL  POTASSIUM  PREDONINE  PROGRAF  RAPAMYCIN  RETROVIR  REVLIMID  SUNITINIB  SUTENT  TAXOL  TAXOTERE  TEMODAR  THALOMID  TOPIRAMATE  TOPOTECAN  TYSABRI  VELCADE  VIREAD  WARFARIN  ZYPREXA  


Bevacizumab Side Effects Report #5651954-7
Health Professional from UNITED STATES reported BEVACIZUMAB problem on Feb 13, 2008. Male patient, 67 years of age, was diagnosed with hepatic neoplasm malignant and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . BEVACIZUMAB dosage: 10 MG/KG, Q2W. During the same period patient was treated with ERLOTINIB, LEVOTHYROXINE, NADOLOL, NORVASC, ALDACTONE, COMPAZINE. Patient was hospitalized. Patient recovered.

Viread Side Effects Report #5677218-3
VIREAD problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Male patient, weighting 11.46 lb, was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . VIREAD dosage: unknown. During the same period patient was treated with FERROUS SULPHATE, VITAMIN CAP, DOMPERIDONE, NITROFURANTOIN, ZIDOVUDINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5631032-3
Consumer or non-health professional from UNITED STATES reported SUTENT problem on Feb 12, 2008. Female patient, weighting 92.59 lb, was diagnosed with malignant melanoma, urinary tract infection and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypotension, . SUTENT dosage: unknown. During the same period patient was treated with BACTRIM, POTASSIUM CHLORIDE, FOSAMAX. Patient was hospitalized. Patient recovered.

Erlotinib Side Effects Report #5632539-5
ERLOTINIB problem was reported by a Health Professional from UNITED STATES on Feb 07, 2008. Female patient, 65 years of age, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, odynophagia, oesophagitis, pain, . ERLOTINIB dosage: 150 MG, ORAL. During the same period patient was treated with BEVACIZUMAB, PACLITAXEL, CARBOPLATIN. Patient was hospitalized. Patient recovered.


Taxol Side Effects Report #5579040-5
Health Professional from UNITED STATES reported TAXOL problem on Dec 31, 2007. Male patient, 63 years of age, weighting 198.4 lb, was diagnosed with adenocarcinoma, hypertension, diabetes mellitus, neutropenia, pain and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypertension, hyponatraemia, neutropenia, sepsis, thrombocytopenia, . TAXOL dosage: RESTARTED ON 28-NOV-07 AT 300MG PRESCRIBED DOSE AT THE TIME OF THE EVENT-200MG. During the same period patient was treated with CARBOPLATIN, ETOPOSIDE, ZESTRIL, GLUCOPHAGE, NEUPOGEN, DARVOCET. Patient was hospitalized. Patient recovered.

Dianeal Side Effects Report #5595520-0
DIANEAL problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Female patient, 84 years of age, was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: failure to thrive, peritonitis, . DIANEAL dosage: unknown. Patient died on 01/12/2008.

Lioresal Side Effects Report #5599151-8
Physician from UNITED STATES reported LIORESAL problem on Jan 09, 2008. Female patient, 69 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: failure to thrive, pneumonia aspiration, pneumonitis, respiratory failure, . LIORESAL dosage: unknown. During the same period patient was treated with LIPITOR, EFFEXOR, VESICARE, ATENOLOL, MAXIMUM GREEN, LEVAQUIN. Patient was hospitalized. Patient died on 12/18/2007.

Tysabri Side Effects Report #5607490-7
TYSABRI problem was reported by a Physician from UNITED STATES on Jan 08, 2008. Female patient, 40 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: failure to thrive, no therapeutic response, . TYSABRI dosage: 300 MG; QM; IV. Patient died.

Taxol Side Effects Report #5608796-8
Health Professional from UNITED STATES reported TAXOL problem on Jan 30, 2008. Male patient, 63 years of age, weighting 198.4 lb, was diagnosed with adenocarcinoma, hypertension, diabetes mellitus, neutropenia, pain and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypertension, hyponatraemia, neutropenia, sepsis, thrombocytopenia, . TAXOL dosage: RESTARTED ON 28-NOV-07 AT 300MG PRESCRIBED DOSE AT THE TIME OF THE EVENT-200MG. During the same period patient was treated with CARBOPLATIN, ETOPOSIDE, ZESTRIL, GLUCOPHAGE, NEUPOGEN, DARVOCET. Patient was hospitalized. Patient recovered.


Lioresal Side Effects Report #5583544-9
LIORESAL problem was reported by a Physician from UNITED STATES on Dec 20, 2007. Female patient, 69 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: failure to thrive, pneumonia aspiration, . LIORESAL dosage: unknown. Patient died on 12/18/2007.

Aredia Side Effects Report #5507287-2
Consumer or non-health professional from JAPAN reported AREDIA problem on Oct 29, 2007. Male patient was diagnosed with osteogenesis imperfecta and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: failure to thrive, inflammation, lower limb fracture, pyrexia, upper limb fracture, . AREDIA dosage: 0.5MG/KG/DOSE X 3 DAYS. Patient recovered.

Predonine Side Effects Report #5481172-7
PREDONINE problem was reported by a Physician from JAPAN on Oct 03, 2007. Female patient, child 6 years of age, weighting 37.48 lb, was diagnosed with rash, chronic myeloid leukaemia and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, headache, hypogammaglobulinaemia, rash, vomiting, . PREDONINE dosage: 7.5 MG/D. During the same period patient was treated with FAMOTIDINE, GLEEVEC. Patient recovered.

Predonine Side Effects Report #5491506-5
Physician from JAPAN reported PREDONINE problem on Oct 11, 2007. Female patient, child 6 years of age, weighting 37.48 lb, was diagnosed with rash, chronic myeloid leukaemia and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, headache, hypogammaglobulinaemia, rash, vomiting, . PREDONINE dosage: 7.5 MG/D. During the same period patient was treated with FAMOTIDINE, GLEEVEC. Patient recovered.

Forteo Side Effects Report #5501605-7
FORTEO problem was reported by a Consumer or non-health professional from FRANCE on Oct 22, 2007. Female patient, 81 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . FORTEO dosage: unknown. Patient died on 10/09/2007.


Bevacizumab Side Effects Report #5444024-4
Health Professional from UNITED KINGDOM reported BEVACIZUMAB problem on Aug 21, 2007. Male patient, weighting 270.9 lb, was diagnosed with bile duct cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hepatic failure, . BEVACIZUMAB dosage: 5 MG/KG, Q2W. During the same period patient was treated with CAPECITABINE, OXALIPLATIN, ALLEGRA, ATIVAN, WELLBUTRIN, MOTRIN, LOVENOX. Patient died on 08/06/2007.

Carboplatin Side Effects Report #5449906-5
CARBOPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient, weighting 120.2 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: failure to thrive, small intestinal obstruction, . CARBOPLATIN dosage: 738 MG. During the same period patient was treated with TAXOTERE, TAXOL. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5463952-7
Consumer or non-health professional from JAPAN reported AREDIA problem on Sept 13, 2007. Male patient, child 9 years of age, was diagnosed with osteogenesis imperfecta and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: failure to thrive, inflammation, lower limb fracture, pyrexia, upper limb fracture, . AREDIA dosage: 0.5MG/KG/DOSE X 3 DAYS. Patient recovered.

Famotidine Side Effects Report #5470565-X
FAMOTIDINE problem was reported by a Physician from JAPAN on Sept 19, 2007. Female patient, child 6 years of age, was diagnosed with chronic myeloid leukaemia and was treated with FAMOTIDINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypogammaglobulinaemia, rash, vomiting, . FAMOTIDINE dosage: 10 MG/D. During the same period patient was treated with GLEEVEC. Patient recovered.

Aredia Side Effects Report #5403594-2
Consumer or non-health professional from JAPAN reported AREDIA problem on July 24, 2007. Male patient was diagnosed with osteogenesis imperfecta and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: failure to thrive, inflammation, lower limb fracture, pyrexia, upper limb fracture, . AREDIA dosage: 0.5MG/KG/DOSE X 3 DAYS. Patient recovered.


Lovenox Side Effects Report #5424912-5
LOVENOX problem was reported by a Physician from UNITED STATES on Aug 23, 2007. Male patient, weighting 270.9 lb, was diagnosed with bile duct cancer and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hepatic failure, . LOVENOX dosage: unknown. During the same period patient was treated with MOTRIN, WELLBUTRIN, ATIVAN, ALLEGRA, AVASTIN, CAPECITABINE, OXALIPLATIN, CHONDORITAN. Patient was hospitalized. Patient died on 08/06/2007.

Prograf Side Effects Report #5383422-4
Physician from JAPAN reported PROGRAF problem on June 28, 2007. Female patient was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: failure to thrive, respiratory failure, . PROGRAF dosage: unknown. Patient died on 11/12/2004.

Didanosine Side Effects Report #5386689-1
DIDANOSINE problem was reported by a Health Professional from UNITED KINGDOM on July 05, 2007. Female patient, weighting 6.61 lb, was diagnosed with human immunodeficiency virus transmission and was treated with DIDANOSINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hepatosplenomegaly, hiv infection, lymphadenopathy, pregnancy, . DIDANOSINE dosage: unknown. During the same period patient was treated with NEVIRAPINE, ZIDOVUDINE. Patient recovered.

Temodar Side Effects Report #5389274-0
Physician from UNITED STATES reported TEMODAR problem on July 05, 2007. Female patient, 68 years of age, weighting 158.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, febrile neutropenia, thrombocytopenia, . TEMODAR dosage: 140 MG; QD; PO. During the same period patient was treated with LIPITOR, DECADRON, PRILOSEC. Patient was hospitalized and became disabled. Patient died on 04/06/2007.

Temodar Side Effects Report #5402393-5
TEMODAR problem was reported by a Physician from UNITED STATES on July 24, 2007. Female patient, 68 years of age, weighting 158.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, febrile neutropenia, thrombocytopenia, . TEMODAR dosage: 140 MG;QD;PO. During the same period patient was treated with LIPITOR, DECADRON, PRILOSEC. Patient was hospitalized and became disabled. Patient died on 04/06/2007.

Prograf Side Effects Report #5383422-4
Physician from JAPAN reported PROGRAF problem on June 28, 2007. Female patient was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: failure to thrive, respiratory failure, . PROGRAF dosage: unknown. Patient died on 11/12/2004.

Didanosine Side Effects Report #5386689-1
DIDANOSINE problem was reported by a Health Professional from UNITED KINGDOM on July 05, 2007. Female patient, weighting 6.61 lb, was diagnosed with human immunodeficiency virus transmission and was treated with DIDANOSINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hepatosplenomegaly, hiv infection, lymphadenopathy, pregnancy, . DIDANOSINE dosage: unknown. During the same period patient was treated with NEVIRAPINE, ZIDOVUDINE. Patient recovered.

Temodar Side Effects Report #5389274-0
Physician from UNITED STATES reported TEMODAR problem on July 05, 2007. Female patient, 68 years of age, weighting 158.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, febrile neutropenia, thrombocytopenia, . TEMODAR dosage: 140 MG; QD; PO. During the same period patient was treated with LIPITOR, DECADRON, PRILOSEC. Patient was hospitalized and became disabled. Patient died on 04/06/2007.

Temodar Side Effects Report #5402393-5
TEMODAR problem was reported by a Physician from UNITED STATES on July 24, 2007. Female patient, 68 years of age, weighting 158.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, febrile neutropenia, thrombocytopenia, . TEMODAR dosage: 140 MG;QD;PO. During the same period patient was treated with LIPITOR, DECADRON, PRILOSEC. Patient was hospitalized and became disabled. Patient died on 04/06/2007.

Effexor Side Effects Report #5759817-3
Health Professional from FRANCE reported EFFEXOR problem on May 29, 2008. Female patient was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypokalaemia, hyponatraemia, urinary retention, . EFFEXOR dosage: 37.5 MG TOTAL DAILY. During the same period patient was treated with PROTHIADEN, ALDACTAZINE. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5767659-8
NEXAVAR problem was reported by a Physician from UNITED STATES on June 10, 2008. Female patient, 59 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with RHINTERLEUKIN, IRON SUPPLEMENT, LORAZEPAM, PAXIL, RITALIN. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5771832-2
Physician from UNITED STATES reported LAPATINIB problem on June 05, 2008. Female patient, 57 years of age, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . LAPATINIB dosage: unknown. During the same period patient was treated with CAPECITABINE. Patient recovered.

Thalomid Side Effects Report #5778827-3
THALOMID problem was reported by a Physician from UNITED STATES on June 10, 2008. Male patient, 89 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . THALOMID dosage: 100 MG, 1 IN 1 D, ORAL. Patient died on 05/15/2008.

Thalomid Side Effects Report #5778975-8
Physician from UNITED STATES reported THALOMID problem on June 10, 2008. Male patient, 89 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . THALOMID dosage: 100 MG, 1 IN 1 D, ORAL. Patient died on 05/15/2008.

Nexavar Side Effects Report #5781366-7
NEXAVAR problem was reported by a Physician from UNITED STATES on June 17, 2008. Female patient, 59 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with RHINTERLEUKIN, IRON SUPPLEMENT, LORAZEPAM, PAXIL, RITALIN. Patient was hospitalized. Patient recovered.

Blopress Side Effects Report #5787406-3
Physician from JAPAN reported BLOPRESS problem on June 18, 2008. Male patient, child 0 years of age, weighting 4.41 lb, was diagnosed with pre-eclampsia and was treated with BLOPRESS. After drug was administered, patient experienced the following problems/side effects: failure to thrive, nephrogenic diabetes insipidus, . BLOPRESS dosage: unknown. Patient recovered.

Oxycontin Side Effects Report #5692217-3
OXYCONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 24, 2008. Female patient was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: failure to thrive, malnutrition, respiratory failure, . OXYCONTIN dosage: unknown. During the same period patient was treated with CYCLOSPORINE, DIFLUCAN, DUONEB, EFFEXOR, FERROUS SULPHATE, ASCORBIC ACID, FLORINEF, LOPRESSOR. Patient died on 02/18/2008.

Lamotrigine Side Effects Report #5707065-5
Consumer or non-health professional from UNITED KINGDOM reported LAMOTRIGINE problem on Apr 14, 2008. Female patient was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . LAMOTRIGINE dosage: 500MG PER DAY. Patient recovered.

Infliximab Side Effects Report #5723337-2
INFLIXIMAB problem was reported by a Health Professional from UNITED STATES on Apr 21, 2008. Male patient, weighting 123.5 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . INFLIXIMAB dosage: unknown. During the same period patient was treated with MERCAPTOPURINE. Patient was hospitalized. Patient recovered.

Rapamycin Side Effects Report #5357397-8
Health Professional from UNITED STATES reported RAPAMYCIN problem on June 12, 2007. Male patient, 57 years of age, weighting 193.3 lb, was diagnosed with pancreatic carcinoma metastatic and was treated with RAPAMYCIN. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hypotension, international normalised ratio increased, . RAPAMYCIN dosage: 5 MG DAILY PO. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5358985-5
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient, 85 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . BONIVA dosage: unknown. Patient died.

Desflurane Side Effects Report #5363246-4
Physician from UNITED STATES reported DESFLURANE problem on June 18, 2007. Female patient, 50 years of age, was treated with DESFLURANE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hepatitis cholestatic, liver injury, . DESFLURANE dosage: unknown. During the same period patient was treated with LEVOFLOXACIN, INSULIN, TYLENOL, MORPHINE, ZOFRAN, SINGULAIR, ALBUTEROL, ATROVENT. Patient recovered.

Bevacizumab Side Effects Report #5328030-6
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on May 17, 2007. Female patient, weighting 123.5 lb, was diagnosed with breast cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . BEVACIZUMAB dosage: 15 MG/KG, Q3W. Patient was hospitalized and became disabled. Patient recovered.

Topiramate Side Effects Report #5334739-0
Physician from UNITED STATES reported TOPIRAMATE problem on Feb 28, 2007. Female patient, weighting 14.99 lb, was diagnosed with partial seizures, convulsion and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: failure to thrive, . TOPIRAMATE dosage: unknown. During the same period patient was treated with KEPPRA, KLONOPIN. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5292434-0
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2007. Female patient, weighting 207.2 lb, was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: failure to thrive, oesophagitis, . BEVACIZUMAB dosage: 10 MG/KG, Q28D. During the same period patient was treated with IRINOTECAN, CARBOPLATIN, VYTORIN, ATACAND, PREMARIN, LUNESTA, MELOXICAM, SERTRALINE. Patient was hospitalized. Patient recovered.

Deroxat Side Effects Report #5296216-5
Consumer or non-health professional from FRANCE reported DEROXAT problem on Apr 04, 2007. Female patient, 92 years of age, was treated with DEROXAT. After drug was administered, patient experienced the following problems/side effects: failure to thrive, hyponatraemia, sinus bradycardia, . DEROXAT dosage: unknown. During the same period patient was treated with INDAPAMIDE, TARKA, VISKEN, CREON, KARDEGIC, ATARAX. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5646345-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 21, 2008. Female patient, weighting 160.0 lb, was diagnosed with neuralgia and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: dehydration, failure to thrive, vomiting, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM. Patient was hospitalized. Patient died on 05/09/2007.

Dianeal Side Effects Report #5655600-8
Health Professional from UNITED STATES reported DIANEAL problem on Feb 29, 2008. Female patient, 84 years of age, was diagnosed with peritoneal dialysis, diabetes mellitus and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, failure to thrive, . DIANEAL dosage: unknown. During the same period patient was treated with INSULIN. Patient was hospitalized. Patient died on 02/06/2008.

Emend Side Effects Report #5662701-7
EMEND problem was reported by a Health Professional from UNITED STATES on Mar 10, 2008. Female patient, 62 years of age, weighting 161.0 lb, was diagnosed with colon cancer metastatic and was treated with EMEND. After drug was administered, patient experienced the following problems/side effects: anorexia, failure to thrive, mental status changes, rectal haemorrhage, . EMEND dosage: 125MG, 80MG, 80MG 3 DAYS WITH EACH PO. During the same period patient was treated with PALONONESTRON. Patient died on 02/25/2008.

Amevive Side Effects Report #5678860-6
Physician from UNITED STATES reported AMEVIVE problem on Mar 07, 2008. Female patient, 44 years of age, weighting 121.0 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, failure to thrive, gastroenteritis radiation, hypokalaemia, nausea, squamous cell carcinoma, vomiting, weight decreased, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Erlotinib Side Effects Report #5679317-9
ERLOTINIB problem was reported by a Physician from UNITED STATES on Mar 06, 2008. Male patient, 67 years of age, was diagnosed with hepatic neoplasm malignant and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: dehydration, failure to thrive, hepatic cirrhosis, hepatic failure, hypotension, . ERLOTINIB dosage: (100 MG,QD), ORAL. During the same period patient was treated with BEVACIZUMAB, LEVOTHYROXINE, NADOLOL, NORVASC, ALDACTONE, COMPAZINE. Patient was hospitalized. Patient recovered.

Paclitaxel Side Effects Report #5579041-7
Health Professional from UNITED STATES reported PACLITAXEL problem on Dec 31, 2007. Male patient, 54 years of age, weighting 233.7 lb, was diagnosed with non-small cell lung cancer and was treated with PACLITAXEL. After drug was administered, patient experienced the following problems/side effects: dehydration, failure to thrive, . PACLITAXEL dosage: TOTAL DOSE 456 MG.CYCLE 3. During the same period patient was treated with CARBOPLATIN, WARFARIN, CODEINE, ULTRAM, LEXAPRO, AMBIEN, NEXIUM. Patient was hospitalized. Patient recovered.

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