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Apidra Side Effects Report #5676846-9
Physician from UNITED STATES reported APIDRA problem on Mar 17, 2008. Female patient, weighting 115.0 lb, was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacteriuria, blood bicarbonate decreased, blood creatine phosphokinase mb increased, blood gases abnormal, blood glucose increased, blood ketone body increased, blood ph decreased, carbon dioxide decreased, . APIDRA dosage: unknown. Patient was hospitalized. Patient recovered.

Apidra Side Effects Report #5625769-X
APIDRA problem was reported by a Physician from UNITED STATES on Feb 05, 2008. Female patient, weighting 115.0 lb, was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacteriuria, blood bicarbonate decreased, blood creatine phosphokinase mb increased, blood gases abnormal, blood glucose increased, blood ketone body increased, blood ph decreased, carbon dioxide decreased, . APIDRA dosage: unknown. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5614685-5
Physician from UNITED STATES reported IBUPROFEN problem on Jan 17, 2008. Female patient, 17 years of age, was diagnosed with overdose and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, av dissociation, blood glucose decreased, blood lactic acid increased, body temperature decreased, brain oedema, continuous haemodiafiltration, depressed level of consciousness, disseminated intravascular coagulation, . IBUPROFEN dosage: unknown. During the same period patient was treated with SERTRALINE, ALBUTEROL. Patient was hospitalized. Patient died.

Fortamet Side Effects Report #5581493-3
FORTAMET problem was reported by a Health Professional from UNITED STATES on Dec 17, 2007. Female patient, 78 years of age, was diagnosed with type 2 diabetes mellitus and was treated with FORTAMET. After drug was administered, patient experienced the following problems/side effects: anion gap increased, dialysis, lactic acidosis, metabolic acidosis, renal injury, . FORTAMET dosage: 1500 MG, BID. During the same period patient was treated with GLYBURIDE, ROFECOXIB, FUROSEMIDE, LEVOTHYROXINE, PREDNISONE, AZATHIOPRINE, PROPRANOLOL. Patient was hospitalized. Patient recovered.


Lorazepam Side Effects Report #5467609-8
Physician from UNITED STATES reported LORAZEPAM problem on Sept 10, 2007. Male patient, 54 years of age, was diagnosed with alcohol withdrawal syndrome and was treated with LORAZEPAM. After drug was administered, patient experienced the following problems/side effects: anion gap increased, haemodialysis, hyperosmolar state, metabolic acidosis, renal injury, . LORAZEPAM dosage: APPROXIMATELY 10-20 MG/HR, NOT REPORTED, INTRAVENOUS DRIP. During the same period patient was treated with INTRAVENOUS FLUIDS, THIAMINE, VITAMIN. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5473386-7
CIPROFLOXACIN problem was reported by a Physician from UNITED STATES on Aug 29, 2007. Female patient, 20 years of age, was diagnosed with bronchopneumonia and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, azotaemia, biopsy kidney abnormal, blood bicarbonate decreased, cough, decreased appetite, fatigue, flank pain, . CIPROFLOXACIN dosage: 1500 MG (750 MG). During the same period patient was treated with TOBRAMYCIN, PULMOZYME, PANCREATIC, CONTRACEPTIVE ORAL. Patient was hospitalized. Patient recovered.

Avandia Side Effects Report #5381988-1
Physician from AUSTRALIA reported AVANDIA problem on June 27, 2007. Male patient, 79 years of age, weighting 224.9 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood alkaline phosphatase increased, blood bicarbonate increased, blood cholesterol decreased, blood creatinine increased, blood glucose increased, blood lactate dehydrogenase increased, blood triglycerides increased, blood urea increased, . AVANDIA dosage: 4MG TWICE PER DAY. During the same period patient was treated with DIAMICRON, ZOCOR, TENORMIN, LASIX, DARBEPOETIN ALFA. Patient recovered.

Avandia Side Effects Report #5381988-1
AVANDIA problem was reported by a Physician from AUSTRALIA on June 27, 2007. Male patient, 79 years of age, weighting 224.9 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood alkaline phosphatase increased, blood bicarbonate increased, blood cholesterol decreased, blood creatinine increased, blood glucose increased, blood lactate dehydrogenase increased, blood triglycerides increased, blood urea increased, . AVANDIA dosage: 4MG TWICE PER DAY. During the same period patient was treated with DIAMICRON, ZOCOR, TENORMIN, LASIX, DARBEPOETIN ALFA. Patient recovered.

Metformin Side Effects Report #5779586-0
Health Professional from TAIWAN, PROVINCE OF CHINA reported METFORMIN problem on June 02, 2008. Female patient, 28 years of age, was diagnosed with weight control and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, intentional overdose, lactic acidosis, metabolic acidosis, suicide attempt, . METFORMIN dosage: 500 MG, ORAL; 39.50 G, OVERDOSE (APPROX., 80 TABLETS). Patient was hospitalized. Patient recovered.


Apidra Side Effects Report #5739507-3
APIDRA problem was reported by a Physician from UNITED STATES on May 12, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacteriuria, blood bicarbonate decreased, blood creatine phosphokinase mb increased, blood gases abnormal, blood glucose increased, blood ketone body increased, blood ph decreased, carbon dioxide decreased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Floxacillin Side Effects Report #5759325-X
Physician from NETHERLANDS reported FLOXACILLIN problem on May 19, 2008. Female patient, 52 years of age, was diagnosed with staphylococcal infection, pain and was treated with FLOXACILLIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, metabolic acidosis, metastasis, respiratory distress, . FLOXACILLIN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient recovered.

Apidra Side Effects Report #5712983-8
APIDRA problem was reported by a Physician from UNITED STATES on Apr 14, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacteriuria, blood bicarbonate decreased, blood creatine phosphokinase mb increased, blood gases abnormal, blood glucose increased, blood ketone body increased, blood ph decreased, carbon dioxide decreased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5713044-4
Consumer or non-health professional from UNITED KINGDOM reported ACETAMINOPHEN problem on Apr 09, 2008. Male patient, 53 years of age, was diagnosed with analgesia and was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood albumin increased, blood alkaline phosphatase increased, blood chloride increased, blood sodium increased, disorientation, metabolic acidosis, myocardial infarction, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with DICLOFENAC, AMOXICILLIN, GENTAMICIN, METRONIDAZOLE, LEVOFLOXACIN, VANCOMYCIN, OMEPRAZOLE, METOCLOPRAMIDE. Patient was hospitalized. Patient died.

Acetaminophen Side Effects Report #5714510-8
ACETAMINOPHEN problem was reported by a Health Professional from UNITED KINGDOM on Apr 09, 2008. Female patient, 82 years of age, was diagnosed with analgesia and was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, ataxia, blood albumin decreased, blood alkaline phosphatase increased, blood magnesium decreased, confusional state, depressed level of consciousness, metabolic acidosis, metabolic encephalopathy, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with FLOXACILLIN, RIFAMPICIN, LEVOFLOXACIN. Patient was hospitalized. Patient recovered.


Apidra Side Effects Report #5721033-9
Physician from UNITED STATES reported APIDRA problem on Apr 22, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacteriuria, blood bicarbonate decreased, blood creatine phosphokinase mb increased, blood gases abnormal, blood glucose increased, blood ketone body increased, blood ph decreased, carbon dioxide decreased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Lorazepam Side Effects Report #5729048-1
LORAZEPAM problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Apr 15, 2008. Male patient, 62 years of age, was diagnosed with sedation and was treated with LORAZEPAM. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bradyarrhythmia, cardiac pacemaker insertion, haemodialysis, lactic acidosis, metabolic acidosis, therapeutic agent toxicity, . LORAZEPAM dosage: 10 MG INTRAVENOUS. During the same period patient was treated with ANTIBIOTICS, MIDAZOLAM. Patient was hospitalized. Patient recovered.

Xopenex Side Effects Report #5363016-7
Physician from UNITED STATES reported XOPENEX problem on June 05, 2007. Male patient, 48 years of age, weighting 228.6 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with XOPENEX. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood glucose increased, small intestinal obstruction, . XOPENEX dosage: unknown. During the same period patient was treated with ALBUTEROL, LORTAB, WELLBUTRIN, NABUMETONE, PROTONIX, ALTACE, AVINZA, ALLEGRA. Patient was hospitalized. Patient recovered.

Xopenex Side Effects Report #5363126-4
XOPENEX HFA problem was reported by a Physician from UNITED STATES on June 05, 2007. Male patient, 48 years of age, weighting 228.6 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with XOPENEX HFA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood glucose increased, neutrophil percentage increased, small intestinal obstruction, white blood cell count increased, . XOPENEX HFA dosage: unknown. During the same period patient was treated with ALBUTEROL, LORTAB, WELLBUTRIN, NABUMETONE, PROTONIX, ALTACE, AVINZA, ALLEGRA. Patient was hospitalized. Patient recovered.

Isoniazid Side Effects Report #5368284-3
Consumer or non-health professional from UNITED STATES reported ISONIAZID problem on June 04, 2007. Male patient, 25 years of age, was diagnosed with pulmonary tuberculosis and was treated with ISONIAZID. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood creatinine increased, blood glucose increased, blood ph decreased, heart rate increased, intentional overdose, liver function test abnormal, . ISONIAZID dosage: 30 TABLETS OF 300 MG. During the same period patient was treated with RIFAMPIN, ETHAMBUTOL, PYRAZINAMIDE, PYRIDOXINE. Patient was hospitalized. Patient recovered.


Avandia Side Effects Report #5369530-2
AVANDIA problem was reported by a Physician from AUSTRALIA on June 15, 2007. Male patient, 79 years of age, weighting 224.9 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood alkaline phosphatase increased, blood bicarbonate increased, blood cholesterol decreased, blood creatinine increased, blood glucose increased, blood lactate dehydrogenase increased, blood triglycerides increased, blood urea increased, . AVANDIA dosage: 4MG TWICE PER DAY. During the same period patient was treated with DIAMICRON, ZOCOR, TENORMIN, LASIX. Patient recovered.

Metformin Side Effects Report #5377761-0
Consumer or non-health professional from UNITED KINGDOM reported METFORMIN problem on June 14, 2007. Female patient, 61 years of age, was diagnosed with diabetes mellitus non-insulin-dependent, pain, coagulopathy and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood glucose increased, blood potassium increased, blood pressure decreased, blood sodium decreased, gingival bleeding, haemodialysis, lactic acidosis, . METFORMIN dosage: unknown. During the same period patient was treated with ROFECOXIB, COUMADIN, FUROSEMIDE, RAMIPRIL. Patient was hospitalized. Patient recovered.

Quetiapine Side Effects Report #5328284-6
QUETIAPINE FUMARATE problem was reported by a Pharmacist from UNITED STATES on May 15, 2007. Male patient, weighting 304.2 lb, was diagnosed with anxiety, schizophrenia and was treated with QUETIAPINE FUMARATE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood glucose increased, diarrhoea, lethargy, nausea, polydipsia, vomiting, . QUETIAPINE FUMARATE dosage: 50 MG QHS (PO). During the same period patient was treated with QUETIAPINE FUMARATE, HYDROCHLOROTHIAZIDE, IBUPROFEN. Patient was hospitalized. Patient recovered.

Truvada Side Effects Report #5333191-9
Consumer or non-health professional from UNITED STATES reported TRUVADA problem on May 21, 2007. Female patient, 33 years of age, weighting 103.0 lb, was diagnosed with hiv infection and was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: anion gap increased, bacterial infection, fungus stool identified, haemodialysis, incorrect dose administered, pulmonary embolism, renal failure acute, urine analysis abnormal, . TRUVADA dosage: 200MG/300MG DAILY PO. During the same period patient was treated with NEVIRAPINE, BACTRIM, VITAMIN B CAP, MUTIVITAMIN, AQUEOUS CREAM, NURISTERATE CONTRACEPTION, CANDICIDE, FUNGIZONE LOZENGES. Patient died on 12/14/2006.

Metformin Side Effects Report #5339669-6
METFORMIN problem was reported by a Physician from UNITED STATES on May 17, 2007. Male patient, 64 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, artery dissection, blood lactic acid increased, blood urea increased, body temperature decreased, dizziness, heart rate increased, hypovolaemia, lactic acidosis, . METFORMIN dosage: 500 MG; BID;. During the same period patient was treated with LEVOTHYROXINE, MECLIZINE, NICOTINIC ACID, NORTRIPTYLINE, SIMVASTATIN, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5292065-2
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Apr 06, 2007. Female patient, weighting 185.2 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, electrolyte imbalance, hyperphosphataemia, metabolic acidosis, renal failure acute, . CISPLATIN dosage: 100 MG. During the same period patient was treated with NAVELBINE, AUGMENTIN, CIPRO, FEXERIL, IBUPROFEN, NEUPOGEN, PERCOSET. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5300312-3
CLOZAPINE problem was reported by a Health Professional from UNITED STATES on Apr 11, 2007. Male patient, 45 years of age, was diagnosed with schizoaffective disorder and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood glucose increased, blood ketone body increased, blood ph decreased, diabetes mellitus, diabetic ketoacidosis, glycosylated haemoglobin increased, . CLOZAPINE dosage: 400 MG/D. During the same period patient was treated with LISINOPRIL, WARFARIN, FUROSEMIDE. Patient died.

Clozapine Side Effects Report #5300337-8
Consumer or non-health professional from UNITED STATES reported CLOZAPINE problem on Apr 11, 2007. Male patient, 29 years of age, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood glucose increased, blood ketone body increased, blood ph decreased, diabetes mellitus, diabetic ketoacidosis, myocardial infarction, urine ketone body present, . CLOZAPINE dosage: 400 MG/D. During the same period patient was treated with DIVALPROEX. Patient died.

Clozapine Side Effects Report #5301706-2
CLOZAPINE problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2007. Male patient, 29 years of age, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood glucose increased, blood ketone body increased, blood ph decreased, diabetes mellitus, diabetic ketoacidosis, myocardial infarction, urine ketone body present, . CLOZAPINE dosage: 400 MG/D. During the same period patient was treated with DIVALPROEX. Patient died.

Olanzapine Side Effects Report #5306887-2
Health Professional from UNITED STATES reported OLANZAPINE problem on Apr 11, 2007. Male patient, 34 years of age, was diagnosed with schizoaffective disorder and was treated with OLANZAPINE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood glucose increased, diabetes mellitus, diabetic ketoacidosis, glycosylated haemoglobin increased, urine ketone body present, . OLANZAPINE dosage: 20 MG/D. During the same period patient was treated with LITHIUM CARBONATE, LAMOTRIGINE, CARBAMAZEPINE. Patient recovered.

Ibuprofen Side Effects Report #5309214-X
IBUPROFEN problem was reported by a Health Professional from UNITED STATES on Apr 04, 2007. Male patient, 14 years of age, weighting 165.3 lb, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, cardiac enzymes increased, coma, extrasystoles, gastrointestinal haemorrhage, hepatic enzyme increased, hypotension, metabolic acidosis, no therapeutic response, . IBUPROFEN dosage: unknown. Patient was hospitalized. Patient recovered.

Quetiapine Side Effects Report #5266041-X
Pharmacist from UNITED STATES reported QUETIAPINE FUMARATE problem on Mar 13, 2007. Male patient, 45 years of age, weighting 228.8 lb, was diagnosed with bipolar disorder and was treated with QUETIAPINE FUMARATE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, condition aggravated, diabetes mellitus inadequate control, fatigue, hyperglycaemia, influenza like illness, polyuria, vision blurred, weight increased, . QUETIAPINE FUMARATE dosage: 150MG PO HS. Patient recovered.

Metformin Side Effects Report #5274550-2
METFORMIN HYDROCHLORIDE problem was reported by a Consumer or non-health professional from NORWAY on Mar 06, 2007. Female patient, 49 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, circulatory collapse, gastroenteritis, haemodialysis, hyperventilation, hypoglycaemia, hypothermia, loss of consciousness, . METFORMIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with GLIBENCLAMIDE, LOSARTAN POSTASSIUM, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Truvada Side Effects Report #5650021-6
Consumer or non-health professional from FRANCE reported TRUVADA problem on Feb 21, 2008. Male patient, weighting 132.3 lb, was diagnosed with hiv infection, antifungal prophylaxis, tuberculosis and was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: agitation, anion gap increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, bundle branch block right, catheter thrombosis, cor pulmonale acute, deep vein thrombosis, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, BACTRIM, RIFADIN, RIMIFON, HEPARIN, MYAMBUTOL. Patient was hospitalized. Patient recovered.

Benadryl Side Effects Report #5682893-3
BENADRYL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient, 23 years of age, was diagnosed with suicide attempt and was treated with BENADRYL. After drug was administered, patient experienced the following problems/side effects: alcohol poisoning, anion gap increased, blood sodium increased, cognitive disorder, depressed level of consciousness, depression, disease recurrence, dizziness, dysthymic disorder, . BENADRYL dosage: unknown. During the same period patient was treated with EXCEDRIN P, CELEXA, ALCOHOL. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5615342-1
Physician from UNITED STATES reported IBUPROFEN problem on Jan 17, 2008. Female patient, 17 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anion gap increased, aspartate aminotransferase increased, av dissociation, blood bicarbonate decreased, blood glucose decreased, brain oedema, computerised tomogram abnormal, depressed level of consciousness, . IBUPROFEN dosage: unknown. During the same period patient was treated with SERTRALINE, ALBUTEROL. Patient was hospitalized. Patient died.

Diltiazem Side Effects Report #5617361-8
DILTIAZEM problem was reported by a Consumer or non-health professional from SPAIN on Jan 16, 2008. Male patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with DILTIAZEM. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anion gap increased, anuria, arteriogram coronary abnormal, blood glucose increased, blood potassium increased, blood sodium decreased, cardiac arrest, . DILTIAZEM dosage: unknown. During the same period patient was treated with METFORMIN, CONTRAST MEDIA, GLYBURIDE, ASPIRIN, RAMIPRIL, NITROGLYCERIN, CLOPIDOGREL, TORSEMIDE. Patient died.

Valproic Side Effects Report #5623302-X
Physician from UNITED STATES reported VALPROIC ACID problem on Jan 07, 2008. Male patient, 27 years of age, was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, anion gap increased, blood pressure diastolic decreased, calcium ionised decreased, completed suicide, hypothermia, hypoxia, miosis, . VALPROIC ACID dosage: unknown. Patient was hospitalized. Patient died.

Modafinil Side Effects Report #5527177-9
MODAFINIL problem was reported by a Health Professional from UNITED STATES on Nov 13, 2007. Female patient, 35 years of age, was treated with MODAFINIL. After drug was administered, patient experienced the following problems/side effects: acidosis, anion gap increased, coma, conduction disorder, hypotension, lethargy, somnolence, suicide attempt, tachycardia, . MODAFINIL dosage: unknown. Patient was hospitalized. Patient recovered.

Amoxicillin Side Effects Report #5701403-5
Consumer or non-health professional from FRANCE reported AMOXICILLIN TRIHYDRATE problem on Mar 25, 2008. Female patient, 69 years of age, weighting 99.21 lb, was treated with AMOXICILLIN TRIHYDRATE. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood bicarbonate decreased, blood creatinine increased, c-reactive protein increased, hyperglycaemia, ketoacidosis, pyrexia, renal failure acute, . AMOXICILLIN TRIHYDRATE dosage: 500 MG, TWICE EVERY 12 HOURS, ORAL. During the same period patient was treated with PNEUMOREL, DETURGYLONE, STAGID, ACETYLCYSTEINE. Patient was hospitalized. Patient recovered.

Vfend Side Effects Report #5711728-5
VFEND problem was reported by a Pharmacist from AUSTRALIA on Apr 09, 2008. Male patient, weighting 176.4 lb, was diagnosed with antifungal prophylaxis, evidence based treatment, pneumocystis jiroveci pneumonia and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anion gap increased, blood albumin decreased, blood alkaline phosphatase increased, blood bicarbonate increased, blood bilirubin increased, blood calcium decreased, blood creatine phosphokinase decreased, blood creatinine increased, . VFEND dosage: unknown. During the same period patient was treated with BACTRIM, VINCRISTINE, PREDNISOLONE. Patient recovered.

Propofol Side Effects Report #5363595-X
Pharmacist from UNITED STATES reported PROPOFOL problem on June 18, 2007. Female patient, 21 years of age, weighting 119.0 lb, was diagnosed with sedation and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: agitation, anion gap increased, blood lactic acid increased, . PROPOFOL dosage: unknown. Patient recovered.

Acetaminophen Side Effects Report #5324415-2
ACETAMINOPHEN problem was reported by a Health Professional from INDIA on Apr 24, 2007. Male patient, 50 years of age, was diagnosed with analgesic effect and was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anion gap increased, barrett's oesophagus, empyema, glomerulonephritis proliferative, haemorrhage, hiatus hernia, lung neoplasm, metabolic acidosis, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with PHENYTOIN, PHENOBARBITONE, CARBAMAZEPINE, STREPTOKINASE, FENTANYL, VANCOMYCIN HYDROCHLORIDE, BICARBONATE. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5324872-1
Consumer or non-health professional from GERMANY reported METFORMIN problem on May 04, 2007. Female patient, 65 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, anion gap increased, gamma-glutamyltransferase increased, . METFORMIN dosage: unknown. Patient was hospitalized. Patient recovered.

Humulin Side Effects Report #5290674-8
HUMULIN problem was reported by a Pharmacist from UNITED STATES on Apr 05, 2007. Male patient, 50 years of age, weighting 363.8 lb, was diagnosed with diabetes mellitus insulin-dependent and was treated with HUMULIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anion gap increased, blood glucose increased, nausea, treatment noncompliance, vomiting, . HUMULIN dosage: unknown. During the same period patient was treated with ASPIRIN, HYDROCHLOROTHIAZIDE, NEURONTIN, ZOLOFT, ENALAPRIL, NIFEDIPINE. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5293596-1
Consumer or non-health professional from FRANCE reported METFORMIN problem on Mar 20, 2007. Female patient, 69 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: agitation, anion gap increased, anuria, blood creatinine increased, blood glucose increased, cytolytic hepatitis, haemodialysis, haemodynamic instability, . METFORMIN dosage: unknown. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5550208-7
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 03, 2007. Female patient, 31 years of age, weighting 192.9 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anhedonia, anion gap increased, arthralgia, back pain, cardiac disorder, chest pain, cholecystitis, cholelithiasis, . ACCUTANE dosage: unknown. During the same period patient was treated with XENICAL. Patient was hospitalized and became disabled. Patient recovered.

Lexapro Side Effects Report #5407877-1
Consumer or non-health professional from UNITED STATES reported LEXAPRO problem on July 23, 2007. Male patient, 51 years of age, weighting 177.0 lb, was diagnosed with post-traumatic stress disorder, blood cholesterol increased and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, amnesia, anion gap increased, aspartate aminotransferase increased, asthenia, base excess decreased, blood bicarbonate decreased, blood chloride decreased, blood creatinine increased, . LEXAPRO dosage: 20 MG BID PO. During the same period patient was treated with ZOCOR, COREG, XANAX, BUSPAR, SEROQUEL. Patient was hospitalized. Patient recovered.

Apidra Side Effects Report #5760086-9
APIDRA problem was reported by a Physician from UNITED STATES on June 02, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal tenderness, anion gap increased, asthenia, back pain, bacteriuria, blood bicarbonate decreased, blood gases abnormal, blood glucose increased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Apidra Side Effects Report #5780515-4
Physician from UNITED STATES reported APIDRA problem on June 13, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal tenderness, anion gap increased, asthenia, back pain, bacteriuria, blood bicarbonate decreased, blood gases abnormal, blood glucose increased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Apidra Side Effects Report #5749343-X
APIDRA problem was reported by a Physician from UNITED STATES on May 14, 2008. Female patient was treated with APIDRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal tenderness, anion gap increased, asthenia, back pain, bacteriuria, blood bicarbonate decreased, blood gases abnormal, blood glucose increased, . APIDRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5339596-4
Physician from UNITED STATES reported METFORMIN problem on May 16, 2007. Male patient, 70 years of age, weighting 169.8 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, agitation, anion gap increased, blood calcium decreased, blood glucose increased, blood phosphorus increased, blood potassium increased, blood sodium decreased, c-reactive protein increased, . METFORMIN dosage: unknown. During the same period patient was treated with FUROSEMIDE, ISOSORBIDE MONONITRATE, QUINAPRIL, DICLOFENAC. Patient was hospitalized. Patient recovered.