Menu

• Ask a Health Expert about ABDOMINAL INFECTION
• Post Your Side Effect related to ABDOMINAL INFECTION
• ABDOMINAL INFECTION and FDA Warnings
• ABDOMINAL INFECTION in Patients Wiki
• Report ABDOMINAL INFECTION in Drug Side Effect Survey

ABDOMINAL INFECTION side effect

What is ABDOMINAL INFECTION ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Tenofovir Side Effects Report #5672017-0
Health Professional from UNITED STATES reported TENOFOVIR problem on Mar 17, 2008. Female patient, 41 years of age, weighting 115.7 lb, was diagnosed with hiv infection and was treated with TENOFOVIR. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain, aspiration, blood pressure diastolic decreased, blood sodium decreased, blood urea decreased, cachexia, central nervous system infection, . TENOFOVIR dosage: 300/200 MG DAILY ORAL. During the same period patient was treated with LOPINAVIR AND RITONAVIR, NEVIRAPINE, COTRIMAXOZOLE, ISONIAZID. Patient died on 02/15/2008.

Mirena Side Effects Report #5610533-8
MIRENA problem was reported by a Health Professional from GERMANY on Jan 28, 2008. Female patient, 34 years of age, weighting 119.0 lb, was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain lower, abdominal rebound tenderness, beta haemolytic streptococcal infection, pelvic peritoneal adhesions, procedural pain, pyrexia, uterine rupture, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5614898-2
Health Professional from GERMANY reported MIRENA problem on Jan 28, 2008. Female patient, 34 years of age, weighting 119.0 lb, was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain lower, abdominal rebound tenderness, beta haemolytic streptococcal infection, pelvic peritoneal adhesions, procedural pain, pyrexia, uterine rupture, . MIRENA dosage: unknown. Patient was hospitalized. Patient recovered.

Competact Side Effects Report #5616537-3
COMPETACT problem was reported by a Consumer or non-health professional from SWITZERLAND on Jan 21, 2008. Male patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with COMPETACT. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acute respiratory distress syndrome, cardiac failure, condition aggravated, disease complication, pneumonia, renal failure, septic shock, weight increased, . COMPETACT dosage: 15 MG PIOGLITAZONE AND 850 MG METFORMIN PER ORAL. During the same period patient was treated with ASPIRIN, OLMESARTAN MEDOXOMIL, ALDACTONE, PLAVIX, CONCOR, ZOCOR, LASIX. Patient was hospitalized. Patient died.


Competact Side Effects Report #5621915-2
Consumer or non-health professional from SWITZERLAND reported COMPETACT problem on Jan 21, 2008. Male patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with COMPETACT. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acute respiratory distress syndrome, cardiac failure, haemodynamic instability, pneumonia, pulmonary sepsis, renal failure, renal failure acute, septic shock, . COMPETACT dosage: 15 MG PIOGLITAZONE AND 850 MG METFORMIN PER ORAL. During the same period patient was treated with ASPIRIN, OLMESARTAN MEDOXOMIL, ALDACTONE, PLAVIX, CONCOR, ZOCOR, LASIX. Patient was hospitalized. Patient died.

Capecitabine Side Effects Report #5624811-X
CAPECITABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Male patient, 59 years of age, weighting 203.9 lb, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, blood creatinine increased, blood urea increased, haemoglobin decreased, hyperglycaemia, hyperkalaemia, hypomagnesaemia, phlebitis, renal failure, . CAPECITABINE dosage: unknown. During the same period patient was treated with OXALIPLATIN. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5626847-1
Consumer or non-health professional from UNITED STATES reported TYSABRI problem on Jan 28, 2008. Female patient, 58 years of age, weighting 178.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain, appendicitis, coma, confusional state, diarrhoea, encephalopathy, sepsis, syncope, . TYSABRI dosage: 300 MG; QM; IV. During the same period patient was treated with CELEXA, IMODIUM, CELEBREX, KLONOPIN WAFER, HYDROCHLOROTHIAZIDE, DETROL LA, ASPIRIN, ORAL CALCIUM. Patient was hospitalized. Patient recovered.

Capecitabine Side Effects Report #5581917-1
CAPECITABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 20, 2007. Male patient, 59 years of age, weighting 215.4 lb, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, blood creatinine increased, blood urea increased, haemoglobin decreased, hyperglycaemia, hyperkalaemia, hypomagnesaemia, phlebitis, ureteric obstruction, . CAPECITABINE dosage: unknown. During the same period patient was treated with OXALIPLATIN. Patient was hospitalized. Patient recovered.

Taxotere Side Effects Report #5582786-6
Health Professional from CHINA reported TAXOTERE problem on Dec 27, 2007. Male patient, 80 years of age, weighting 132.3 lb, was diagnosed with hypertension and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, hypoalbuminaemia, intestinal obstruction, pneumonia, . TAXOTERE dosage: unknown. During the same period patient was treated with PREDNISONE, AMLODIPINE BESYLATE. Patient died on 05/19/2007.


Actos Side Effects Report #5584896-6
ACTOS problem was reported by a Physician from UNITED STATES on Dec 27, 2007. Female patient, 63 years of age, weighting 230.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, anxiety, blood glucose decreased, cough, dizziness, ear infection, hernia obstructive, malaise, oedema peripheral, . ACTOS dosage: 15 MG, 1 IN 1 D, PER ORAL; 30 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with OXYTROL, DETROL LA, FLOMAX, ASPIRIN, ZETIA, PREMARIN. Patient recovered.

Mirena Side Effects Report #5605404-7
Consumer or non-health professional from SWEDEN reported MIRENA problem on Jan 17, 2008. Female patient, 45 years of age, was diagnosed with hypertension and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, ovarian infection, pain, pyrexia, . MIRENA dosage: unknown. During the same period patient was treated with SELOKEN. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5534264-8
REMICADE problem was reported by a Health Professional from UNITED KINGDOM on Nov 26, 2007. Female patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, osteoarthritis, osteoporosis, sepsis, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISOLONE, ALENDRONATE, ETORICOXIB, OMEPRAZOLE. Patient died on 05/06/2007.

Certican Side Effects Report #5517968-2
Physician from UNITED STATES reported CERTICAN problem on Nov 07, 2007. Male patient, 59 years of age, weighting 262.4 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, anuria, complications of transplanted kidney, hypotension, ischaemia, myocardial infarction, nephropathy toxic, renal tubular necrosis, urine output decreased, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with PREDNISONE, NEORAL. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5475165-3
FORTEO problem was reported by a Consumer or non-health professional from CANADA on Sept 21, 2007. Male patient, 64 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, cardiac arrest, cardiac failure, chills, nausea, pneumonia, respiratory failure, vomiting, . FORTEO dosage: unknown. During the same period patient was treated with PREDNISONE, FUROSEMIDE, REVASC, ASAPHEN, CLONAZEPAM. Patient was hospitalized. Patient recovered.


Natalizumab Side Effects Report #5478924-6
Health Professional from UNITED STATES reported NATALIZUMAB problem on Sept 18, 2007. Female patient, 58 years of age, weighting 178.0 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: abdominal infection, appendicitis, coma, diverticular perforation, encephalopathy, sepsis, syncope, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with CELEXA, IMODIUM, CELEBREX, KLONOPIN WAFER, HYDROCHLOROTHIAZIDE, DETROL LA, ASPIRIN, CORAL CALCIUM. Patient was hospitalized. Patient recovered.

Leucovorin Side Effects Report #5481159-4
LEUCOVORIN problem was reported by a Physician from UNITED STATES on Sept 27, 2007. Male patient, 43 years of age, was diagnosed with small intestine carcinoma and was treated with LEUCOVORIN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acute monocytic leukaemia, anaemia, intestinal obstruction, post procedural haemorrhage, post procedural infection, sepsis, wound dehiscence, . LEUCOVORIN dosage: 200 MG/M2 PER _CYCLE. During the same period patient was treated with FLUOROURACIL, IRINOTECAN. Patient recovered.

Forteo Side Effects Report #5487130-0
Consumer or non-health professional from CANADA reported FORTEO problem on Oct 04, 2007. Male patient, 64 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, cardiac arrest, cardiac failure, chills, haematochezia, nausea, pneumonia, respiratory failure, vomiting, . FORTEO dosage: unknown. During the same period patient was treated with PREDNISONE, FUROSEMIDE, REVASC, ASAPHEN, CLONAZEPAM. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5489218-7
ACTOS problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 02, 2007. Female patient, 63 years of age, weighting 230.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal strangulated hernia, accident, blood glucose decreased, blood glucose increased, dizziness, malaise, sudden onset of sleep, weight increased, . ACTOS dosage: 30 MG, 1 IN 1 D, PER ORAL; 30 MG, 1/2 TABLET, 1 IN 1 D, PER ORAL. During the same period patient was treated with OXYTROL, DETROL. Patient recovered.

Basiliximab Side Effects Report #5467781-X
Health Professional from BELGIUM reported BASILIXIMAB problem on Sept 20, 2007. Male patient, 52 years of age, was diagnosed with renal and pancreas transplant and was treated with BASILIXIMAB. After drug was administered, patient experienced the following problems/side effects: abdominal infection, aspergillosis, atelectasis, blood bicarbonate decreased, blood creatinine increased, bronchial disorder, bronchopulmonary aspergillosis, c-reactive protein increased, cardiac failure, . BASILIXIMAB dosage: 30 MG, ONCE/SINGLE. During the same period patient was treated with METHYLPREDNISOLONE, TACROLIMUS, MYCOPHENOLATE MOFETIL. Patient was hospitalized. Patient died.


Boniva Side Effects Report #5469392-9
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 19, 2007. Female patient, 47 years of age, weighting 179.9 lb, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, renal failure, . BONIVA dosage: unknown. During the same period patient was treated with TRICOR, LIPITOR, METFORMIN, GLYBURIDE. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5469393-0
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Sept 19, 2007. Female patient, 47 years of age, weighting 179.9 lb, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, renal failure, . BONIVA dosage: unknown. During the same period patient was treated with TRICOR, LIPITOR, METFORMIN, GLYBURIDE. Patient was hospitalized. Patient recovered.

Irinotecan Side Effects Report #5406508-4
IRINOTECAN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 01, 2007. Female patient, 56 years of age, was diagnosed with colorectal cancer metastatic and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain lower, acute respiratory distress syndrome, ascites, asthenia, decubitus ulcer, fatigue, fistula, hypotension, . IRINOTECAN dosage: DAILY DOSE:240MG-FREQ:FREQUENCY: ONCE EVERY 2 WEEKS. During the same period patient was treated with CETUXIMAB, DIPHENHYDRAMINE HYDROCHLORIDE, PALONOSETRON, DEXAMETHASONE. Patient was hospitalized. Patient died.

Irinotecan Side Effects Report #5411569-2
Consumer or non-health professional from UNITED STATES reported IRINOTECAN problem on Aug 01, 2007. Female patient, 56 years of age, was diagnosed with colorectal cancer metastatic and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal pain lower, acute respiratory distress syndrome, ascites, asthenia, decubitus ulcer, fatigue, fistula, hypotension, . IRINOTECAN dosage: DAILY DOSE:240MG-FREQ:FREQUENCY: ONCE EVERY 2 WEEKS. During the same period patient was treated with CETUXIMAB, DIPHENHYDRAMINE HYDROCHLORIDE, PALONOSETRON, DEXAMETHASONE. Patient was hospitalized. Patient died.

Byetta Side Effects Report #5421274-4
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Female patient, 66 years of age, weighting 165.0 lb, was diagnosed with type 2 diabetes mellitus, gastrooesophageal reflux disease, postmenopause, lipids increased, pain, neuropathy, hypertension and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, colitis ischaemic, diarrhoea, presyncope, vomiting, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with ZANTAC, PREMARIN, LOPID, NAPROXEN, NEURONTIN, LASIX, DILTIAZEM. Patient was hospitalized. Patient recovered.

Cipro Side Effects Report #5426039-5
Physician from UNITED STATES reported CIPRO problem on Aug 24, 2007. Male patient, 53 years of age, weighting 180.0 lb, was treated with CIPRO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abnormal behaviour, anastomotic leak, anxiety, completed suicide, computerised tomogram abdomen abnormal, decreased interest, diverticulitis, fear, . CIPRO dosage: unknown. During the same period patient was treated with FLAGYL. Patient died on 05/31/2007.

Forteo Side Effects Report #5438435-0
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 21, 2007. Female patient, 62 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abscess intestinal, incisional hernia, intestinal perforation, intestinal polyp, procedural pain, . FORTEO dosage: unknown. During the same period patient was treated with PREVACID, AVAPRO, DEMADEX, COREG, ASPIRIN, CALCIUM, ASCORBIC ACID, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5390752-9
Consumer or non-health professional from UNITED STATES reported FORTEO problem on July 05, 2007. Female patient, 62 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abscess intestinal, hernia, intestinal perforation, intestinal polyp, procedural pain, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Metronidazole Side Effects Report #5393316-6
METRONIDAZOLE problem was reported by a Health Professional from UNITED KINGDOM on July 12, 2007. Male patient, 54 years of age, was diagnosed with schizophrenia and was treated with METRONIDAZOLE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, blood albumin decreased, catabolic state, ileus, intestinal functional disorder, laparotomy, life support, malaise, sepsis, . METRONIDAZOLE dosage: unknown. During the same period patient was treated with CLOZARIL. Patient was hospitalized. Patient recovered.

Thymoglobulin Side Effects Report #5402076-1
Physician from UNITED STATES reported THYMOGLOBULIN problem on July 14, 2006. Male patient, 61 years of age, weighting 199.3 lb, was diagnosed with liver transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acidosis, ascites, ascites infection, candidiasis, coagulopathy, continuous haemodiafiltration, convulsion, disseminated intravascular coagulation, . THYMOGLOBULIN dosage: 136 MG ONCE IV. During the same period patient was treated with BACTROBAN, BUMEX, ZOSYN, PROTONIX, LACTULOSE, CHLORIDE, HIBICLENS. Patient was hospitalized. Patient died on 06/25/2006.

Cetuximab Side Effects Report #5402398-4
CETUXIMAB problem was reported by a Health Professional from UNITED STATES on July 30, 2007. Female patient, 56 years of age, weighting 121.7 lb, was diagnosed with rectal cancer metastatic and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acute respiratory distress syndrome, coagulopathy, decubitus ulcer, hypotension, hypoxia, ileal perforation, ileorectal fistula, myocardial infarction, . CETUXIMAB dosage: 900 MG Q2WEEKS INTRAVENOU. During the same period patient was treated with IRINOTECAN, DIPHENHYDRAMINE, PALONOSETRON, DEXAMETHASONE, VITAMIN D, ASCORBIC ACID, VITAMIN B, VITAMIN B6. Patient was hospitalized. Patient died on 06/07/2007.

Dronabinol Side Effects Report #5424222-6
Physician from UNITED STATES reported DRONABINOL problem on Sept 05, 2006. Male patient, weighting 140.0 lb, was diagnosed with decreased appetite and was treated with DRONABINOL. After drug was administered, patient experienced the following problems/side effects: abdominal infection, cytomegalovirus infection, mycobacterium avium complex infection, . DRONABINOL dosage: 2.5 MILLIGRAM(S) BID ORAL DAILY DOSE: 5 MILLIGRAM(S). During the same period patient was treated with VASOTEC, DIFLUCAN, FLOXIN, ELAVIL, BACTRIM DS, INHALED PENTAM, HISMANAL, SELDANE. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5390752-9
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 62 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abscess intestinal, hernia, intestinal perforation, intestinal polyp, procedural pain, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Metronidazole Side Effects Report #5393316-6
Health Professional from UNITED KINGDOM reported METRONIDAZOLE problem on July 12, 2007. Male patient, 54 years of age, was diagnosed with schizophrenia and was treated with METRONIDAZOLE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, blood albumin decreased, catabolic state, ileus, intestinal functional disorder, laparotomy, life support, malaise, sepsis, . METRONIDAZOLE dosage: unknown. During the same period patient was treated with CLOZARIL. Patient was hospitalized. Patient recovered.

Thymoglobulin Side Effects Report #5402076-1
THYMOGLOBULIN problem was reported by a Physician from UNITED STATES on July 14, 2006. Male patient, 61 years of age, weighting 199.3 lb, was diagnosed with liver transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acidosis, ascites, ascites infection, candidiasis, coagulopathy, continuous haemodiafiltration, convulsion, disseminated intravascular coagulation, . THYMOGLOBULIN dosage: 136 MG ONCE IV. During the same period patient was treated with BACTROBAN, BUMEX, ZOSYN, PROTONIX, LACTULOSE, CHLORIDE, HIBICLENS. Patient was hospitalized. Patient died on 06/25/2006.

Cetuximab Side Effects Report #5402398-4
Health Professional from UNITED STATES reported CETUXIMAB problem on July 30, 2007. Female patient, 56 years of age, weighting 121.7 lb, was diagnosed with rectal cancer metastatic and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: abdominal infection, acute respiratory distress syndrome, coagulopathy, decubitus ulcer, hypotension, hypoxia, ileal perforation, ileorectal fistula, myocardial infarction, . CETUXIMAB dosage: 900 MG Q2WEEKS INTRAVENOU. During the same period patient was treated with IRINOTECAN, DIPHENHYDRAMINE, PALONOSETRON, DEXAMETHASONE, VITAMIN D, ASCORBIC ACID, VITAMIN B, VITAMIN B6. Patient was hospitalized. Patient died on 06/07/2007.

Dronabinol Side Effects Report #5424222-6
DRONABINOL problem was reported by a Physician from UNITED STATES on Sept 05, 2006. Male patient, weighting 140.0 lb, was diagnosed with decreased appetite and was treated with DRONABINOL. After drug was administered, patient experienced the following problems/side effects: abdominal infection, cytomegalovirus infection, mycobacterium avium complex infection, . DRONABINOL dosage: 2.5 MILLIGRAM(S) BID ORAL DAILY DOSE: 5 MILLIGRAM(S). During the same period patient was treated with VASOTEC, DIFLUCAN, FLOXIN, ELAVIL, BACTRIM DS, INHALED PENTAM, HISMANAL, SELDANE. Patient was hospitalized. Patient recovered.

Tigecycline Side Effects Report #5755797-5
Physician from GREECE reported TIGECYCLINE problem on May 02, 2007. Male patient, 62 years of age, was diagnosed with abdominal infection and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, . TIGECYCLINE dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5763163-1
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 21, 2008. Female patient, 65 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal mass, decubitus ulcer, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5766680-3
Health Professional from UNITED KINGDOM reported REMICADE problem on May 30, 2008. Female patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, osteoarthritis, osteoporosis, sepsis, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISOLONE, ALENDRONATE, ETORICOXIB, SENNA, CYCLOSPORINE, LACTULOSE, LOSEC I. Patient died on 05/06/2007.

Avonex Side Effects Report #5778286-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on June 05, 2008. Female patient, 39 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal infection, haematoma, precancerous cells present, scar, smear cervix abnormal, vomiting, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5780522-1
Physician from BRAZIL reported HUMIRA problem on June 11, 2008. Female patient, weighting 125.7 lb, was diagnosed with intestinal fistula, crohn's disease, deep vein thrombosis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, adverse event, ataxia, crohn's disease, dizziness, fistula, frequent bowel movements, gait disturbance, gastrointestinal disorder, . HUMIRA dosage: unknown. During the same period patient was treated with WARFARIN, PREDNISONE, METRONIDASOLE, PANTOPRAZOLE, AZATHIOPRINE. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5735735-1
MIRENA problem was reported by a Consumer or non-health professional from SWEDEN on May 05, 2008. Female patient, 45 years of age, was diagnosed with hypertension and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, ovarian infection, pain, pelvic infection, pyrexia, . MIRENA dosage: unknown. During the same period patient was treated with SELOKEN. Patient was hospitalized. Patient recovered.

Cancidas Side Effects Report #5742508-2
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported CANCIDAS problem on May 01, 2008. Female patient, 79 years of age, was diagnosed with candidiasis and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, alanine aminotransferase increased, ascites, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, enterococcal bacteraemia, hyperbilirubinaemia, incision site infection, . CANCIDAS dosage: 150 MG DAILY IV. During the same period patient was treated with ATROVENT, AZACTAM, BRICANYL, CIPROFLOXACIN, DIFLUCAN, FENTANYL ORALET, FORTUM, FAMOTIDINE. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5692651-1
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2008. Female patient, 65 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal mass, decubitus ulcer, malaise, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Inj Side Effects Report #5724400-2
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported INJ CASPOFUNGIN ACETATE problem on Jan 24, 2007. Female patient, 79 years of age, was diagnosed with candidiasis and was treated with INJ CASPOFUNGIN ACETATE. After drug was administered, patient experienced the following problems/side effects: abdominal infection, alanine aminotransferase increased, ascites, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, enterococcal bacteraemia, hyperbilirubinaemia, . INJ CASPOFUNGIN ACETATE dosage: unknown. During the same period patient was treated with ACETAMINOPHEN, AMLODIPINE BESYLATE, ANTIMICROBIAL, AZTREONAM, CEFTAZIDIME, CIPROFLOXACIN HYDROCHLORIDE, FAMOTIDINE, FENTANYL CITRATE. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5371934-9
TACROLIMUS problem was reported by a Health Professional from UNITED KINGDOM on June 15, 2007. Male patient, 58 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, aspiration tracheal abnormal, asthenia, bone marrow failure, candidiasis, cerebral haemorrhage, continuous haemodiafiltration, convulsion, enterococcal infection, . TACROLIMUS dosage: 3 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, METHYLPREDNISOLONE, PREDNISONE, ANTITHROMBIN II, TRIMETHOPRIM, CALCIUM, CILASTIN W, METAMIZOLE. Patient was hospitalized. Patient died on 09/07/2005.

Humira Side Effects Report #5374644-7
Physician from UNITED STATES reported HUMIRA problem on Mar 20, 2007. Female patient, 60 years of age, weighting 188.0 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: abdominal infection, diarrhoea, vomiting, . HUMIRA dosage: 40 MG, 1 IN 1 WK, SUBCUTANEOUS. During the same period patient was treated with DICYCLOMINE, IMODIUM, KADIAN, VICODIN, LEXAPRO, ERGOCALCIFEROL, CLONAZEPAM. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5376207-6
TACROLIMUS problem was reported by a Health Professional from UNITED KINGDOM on June 18, 2007. Female patient, 59 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, aspergillosis, blood bilirubin increased, bone marrow failure, candidiasis, cholestasis, complications of transplanted liver, enterococcal infection, fungal sepsis, . TACROLIMUS dosage: 4 MG, UID/QD, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DACLIZUMAB, METHYLPREDNISOLONE, PREDNISONE, HYDROCORTISONE, NOREPINEPHRINE HYDROCHLORIDE, ANTITHROMBIN III, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient was hospitalized. Patient died on 09/28/2005.

Forteo Side Effects Report #5315839-8
Consumer or non-health professional from SPAIN reported FORTEO problem on Apr 19, 2007. Female patient, 86 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal infection, coma, intestinal perforation, respiratory failure, skin ulcer, vomiting, . FORTEO dosage: unknown. During the same period patient was treated with ALMAX. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5343399-4
TACROLIMUS problem was reported by a Health Professional from GERMANY on May 18, 2007. Male patient, 58 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, abdominal sepsis, aspiration tracheal abnormal, bone marrow failure, candidiasis, cholestasis, continuous haemodiafiltration, convulsion, enterococcal infection, . TACROLIMUS dosage: 3 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, METHYLPREDNISOLONE, PREDNISONE, ANTITHROMBIN II, TRIMETHOPRIM, CALCIUM CHLORIDE, CILASTATIN W. Patient was hospitalized. Patient died on 09/07/2005.

Tacrolimus Side Effects Report #5343636-6
Health Professional from GERMANY reported TACROLIMUS problem on May 18, 2007. Female patient, 59 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: abdominal infection, aspergillosis, bone marrow failure, candidiasis, enterococcal infection, haematoma infection, hepatic failure, multi-organ failure, post procedural complication, . TACROLIMUS dosage: 0.5 MG, UID/QD, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DACLIZUMAB, METHYLPRENISOLONE, PREDNISONE, HYDROCORTISONE, NOREPINEPHRINE HYDROCHLORIDE, ANTITHROMBIN III, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient was hospitalized. Patient died on 09/28/2005.