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

ALANINE AMINOTRANSFERASE INCREASED ( 50 FDA reports)
HEPATITIS B ( 46 FDA reports)
DRUG RESISTANCE ( 32 FDA reports)
DRUG INEFFECTIVE ( 29 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 28 FDA reports)
ASCITES ( 23 FDA reports)
ASTHENIA ( 19 FDA reports)
HBV DNA INCREASED ( 19 FDA reports)
HEPATIC FAILURE ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
HEPATITIS B DNA INCREASED ( 18 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 17 FDA reports)
HEPATIC CIRRHOSIS ( 17 FDA reports)
HEPATIC ENCEPHALOPATHY ( 17 FDA reports)
HYPOPHOSPHATAEMIA ( 17 FDA reports)
MYALGIA ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
JAUNDICE ( 16 FDA reports)
RENAL INJURY ( 16 FDA reports)
VIRAL INFECTION ( 16 FDA reports)
VOMITING ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
OSTEOMALACIA ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 10 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 10 FDA reports)
BLOOD CALCIUM ABNORMAL ( 10 FDA reports)
BLOOD CREATININE ABNORMAL ( 10 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 10 FDA reports)
BLOOD UREA ABNORMAL ( 10 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PROTEIN TOTAL ABNORMAL ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
VIRAL MUTATION IDENTIFIED ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ACANTHOSIS ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HEPATITIS B VIRUS ( 5 FDA reports)
HYPERLACTACIDAEMIA ( 5 FDA reports)
LIPODYSTROPHY ACQUIRED ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
WOUND ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COUGH ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
LARYNGEAL ERYTHEMA ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
MYALGIA INTERCOSTAL ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
PAIN ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
RASH ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
VIRAEMIA ( 4 FDA reports)
VIRAL HEPATITIS CARRIER ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS E ANTIGEN POSITIVE ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
TRISOMY 13 ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD HIV RNA DECREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B E ANTIGEN ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL GLYCOSURIA ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE PHOSPHORUS INCREASED ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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