Please choose an event type to view the corresponding MedsFacts report:

DIARRHOEA ( 38 FDA reports)
HYPERLIPIDAEMIA ( 36 FDA reports)
HYPERLACTACIDAEMIA ( 31 FDA reports)
PYREXIA ( 30 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 21 FDA reports)
LEUKOENCEPHALOPATHY ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
RASH ( 18 FDA reports)
CACHEXIA ( 17 FDA reports)
LACTIC ACIDOSIS ( 17 FDA reports)
HEPATIC STEATOSIS ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
MASS ( 15 FDA reports)
TACHYCARDIA ( 14 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
DRUG RESISTANCE ( 12 FDA reports)
MALAISE ( 12 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
BLOOD LACTIC ACID INCREASED ( 11 FDA reports)
DEATH ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
LIPODYSTROPHY ACQUIRED ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
TREATMENT NONCOMPLIANCE ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
HEADACHE ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
PSORIASIS ( 10 FDA reports)
AGITATION ( 9 FDA reports)
AIDS ENCEPHALOPATHY ( 9 FDA reports)
ASEPTIC NECROSIS BONE ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 9 FDA reports)
PARKINSONISM ( 9 FDA reports)
VIRAL MUTATION IDENTIFIED ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
ANOGENITAL WARTS ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
GLAUCOMA ( 8 FDA reports)
MONONEUROPATHY ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NEURALGIA ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
ORAL CANDIDIASIS ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
TRIGEMINAL NEURALGIA ( 8 FDA reports)
VIRAL LOAD DECREASED ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
FAT REDISTRIBUTION ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HAEMARTHROSIS ( 7 FDA reports)
IMPETIGO ( 7 FDA reports)
LIP EROSION ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
COUGH ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
VIRAL LOAD INCREASED ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
VISCERAL LEISHMANIASIS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIV WASTING SYNDROME ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AIDS DEMENTIA COMPLEX ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLUCOCORTICOIDS INCREASED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SALIVARY GLAND CYST ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)

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